XY individuals with disorders/differences of sex development (DSD) are characterized by reduced androgenization caused, in some children, by gonadal dysgenesis or testis regression during fetal development. The genetic etiology for most patients with 46,XY gonadal dysgenesis and for all patients with testicular regression syndrome (TRS) is unknown.
We performed exome and/or Sanger sequencing in 145 individuals with 46,XY DSD of unknown etiology including gonadal dysgenesis and TRS.
Thirteen children carried heterozygous missense pathogenic variants involving the RNA helicase DHX37, which is essential for ribosome biogenesis. Enrichment of rare/novel DHX37 missense variants in 46,XY DSD is highly significant compared with controls (P value = 5.8 × 10−10). Five variants are de novo (P value = 1.5 × 10−5). Twelve variants are clustered in two highly conserved functional domains and were specifically associated with gonadal dysgenesis and TRS. Consistent with a role in early testis development, DHX37 is expressed specifically in somatic cells of the developing human and mouse testis.
DHX37 pathogenic variants are a new cause of an autosomal dominant form of 46,XY DSD, including gonadal dysgenesis and TRS, showing that these conditions are part of a clinical spectrum. This raises the possibility that some forms of DSD may be a ribosomopathy.
Disorders/differences of sex development (DSD) are defined as congenital conditions with discordant development of chromosomal and gonadal/anatomical sex and cover a wide range of phenotypes that involve the endocrine and reproductive systems.1 A subgroup of DSD consists of individuals with anomalies of testicular formation or the maintenance of testicular tissue during early embryonic development. The former comprises 46,XY complete or partial gonadal dysgenesis (MIM 400044). The complete form is characterized by female external genitalia, well-developed Müllerian structures, and gonads of fibrous ovarian-like stroma with no evidence of testicular differentiation.2 46,XY partial gonadal dysgenesis is characterized by partially developed internal ducts usually consisting of a mixture of Wolffian (epididymis, vas deferens, and seminal vesicle) and Müllerian ducts (fallopian tube, uterus, and upper third of the vagina) with varying degrees of virilization of the external genitalia depending on the amount of testicular tissue present.2
46,XY testicular regression syndrome (TRS) is defined by a 46,XY chromosome complement, ambiguous or atypical genitalia, anomalies of sexual duct formation, and absence of gonadal tissue on one or both sides (MIM 273250).3,4,5 Some boys with TRS are born with normal external genitalia but present with cryptorchidism and may even have one or both palpable testes that subsequently involute. Children with TRS are considered to have variable degrees of testicular determination with the loss of gonad tissue early in gestation before testis formation is complete. The exact prevalence of TRS is unknown, but has been estimated to affect approximately 1:2000 boys.6 Anorchia is defined by the complete absence of testicular tissue in a 46,XY phenotypic male. However, since male-typical differentiation of the genital tract and the development of the external genitalia are dependent on the production of anti-Müllerian hormone (AMH) and androgens, the testis must have been present at least up to the 16th week of gestation in these individuals.7 In some circumstances anorchia may occur secondary to a vascular event or testicular torsion.8 Bilateral congenital anorchia has a prevalence of approximately 1:20,000 males and unilateral congenital anorchia a prevalence of 1:6500 males.9
Determining the genetic etiology of 46,XY gonadal dysgenesis and 46,XY TRS has been challenging. No gene pathogenic variants have been reported in association with the latter and in the former pathogenic variants in SRY (MIM 480000), NR5A1 (encoding steroidogenic factor-1, SF-1; [MIM 184757]), and MAP3K1 (MIM 600982) are the most prevalent causes, but together explain less than 40% of all 46,XY gonadal dysgenesis.10 Pathogenic variants in other genes including SOX9 (MIM 608160), SOX8 (MIM 605923), GATA4 (MIM 600576), DMRT1 (MIM 602424), FOG2 (MIM 603693), WT1 (MIM 607102), DHH (MIM 605423), CBX2 (MIM 602770), ATRX (MIM 300032), FGF9 (MIM 600921), and ZNRF3 (MIM 612062) are reported in rare individuals as a cause of both syndromic and nonsyndromic forms of 46,XY gonadal dysgenesis as well as some 46,XY boys with severe penoscrotal hypospadias.10,11,12 The families of some patients with TRS raised as male also include other children with complete or partial 46,XY gonadal dysgenesis or agonadism who are raised as female.4,5,13,14 Thus, both 46,XY gonadal dysgenesis and TRS can be regarded as a continuum of phenotypes due to errors in testis determination and maintenance rather than clearly distinct and unrelated categories of atypical testicular formation.14 Though TRS is part of the clinical spectrum of 46,XY gonadal dysgenesis and may share a common genetic etiology, identification of the gene(s) involved has proven elusive.
Here, using exome and Sanger sequencing approaches for 145 individuals with 46,XY DSD of unknown etiology, we identified recurrent pathogenic variants in the DEAH-box RNA helicase DHX37 specifically in association with 46,XY gonadal dysgenesis and 46,XY TRS.
MATERIALS AND METHODS
Patient and control samples
We studied 145 cases with 46,XY DSD of unknown etiology. They were defined as 46,XY gonadal dysgenesis (n = 81), 46,XY TRS (n = 16), 46,XY boys with severe penoscrotal hypospadias (n = 33), and 46,XY anorchia (n = 15). All patients were screened for pathogenic variants in genes known to cause DSD either by analysis of exome data sets or by direct Sanger sequencing of candidate genes. All patients with 46,XY DSD met the revised criteria of the Pediatric Endocrine Society (LWPES)/European Society for Paediatric Endocrinology (ESPE). This study was approved by the local French ethical committee (2014/18NICB—registration number IRB00003835) and consent to genetic testing was obtained from adult probands or from the parents when the patient was under 18 years. Patient ancestry was determined by self reporting, based on responses to a personal questionnaire, which asked questions pertaining to the birthplace, languages, and self-reported ethnicity of the participants, their parents, and grandparents. Genes known to be involved in 46,XY DSD were screened for pathogenic variants in the XY DSD cohort and high-resolution array comparative genomic hybridization (aCGH) was performed on all cases and indicated normal ploidy in all cases.
One hundred patients presenting with 46,XY DSD were sequenced using the exome approach as described elsewhere.11 Exon enrichment was performed with Agilent SureSelect Human All Exon V4. Paired-end sequencing was performed on the Illumina HiSeq2000 platform with TruSeq v3 chemistry. Read files (fastq) were generated from the sequencing platform via the manufacturer’s proprietary software. Reads were mapped with the Burrows–Wheeler Aligner, and local realignment of the mapped reads around potential insertion/deletion (indel) sites was carried out with GATK version 1.6. Duplicate reads were marked with Picard version 1.62 (http://broadinstitute.github.io/picard/). Additional BAM file manipulations were performed with SAMtools (0.1.18). Single-nucleotide polymorphism (SNP) and indel variants were called with the Genome Analysis Toolkit (GATK) Unified Genotyper for each sample. SNP novelty was determined against dbSNP138. Novel variants were analyzed by a range of web-based bioinformatics tools with the EnsEMBL SNP Effect Predictor (http://www.ensembl.org/homosapiens/userdata/uploadvariations). All variants were screened manually against the Human Gene Mutation Database Professional Biobase (http://www.biobase-international.com/product/hgmd/). In silico analysis was performed to determine the potential pathogenicity of the variants. Potentially pathogenic variants were verified with classic Sanger sequencing.
Sanger sequencing of the entire coding sequence of DHX37
Sanger sequencing was performed for the DHX37 gene in 45 patients with 46,XY gonadal dysgenesis (n = 30), 3 patients with testicular regression syndrome, and 12 patients with anorchia. Polymerase chain reaction (PCR) amplification and Sanger sequencing of DHX37 was performed using the primers listed in Table S1. The conditions for PCR were 95 °C for 5 minutes followed by 35 cycles of 95 °C for 30 seconds, 58.5 °C for 30 seconds, and 72 °C for 30 seconds. DNA sequence analysis was performed using at least 200 ng of purified DNA, 20 ng of primer and fluorescently labeled Taq DyeDeoxy terminator reaction mix (Applied Biosystems, Foster City, CA, USA) according to the manufacturer’s instructions. DNA sequence was determined using a 373A automated DNA sequencer (Applied Biosystems).
The homologous 2.6 Å crystal structure of Prp43-ADP-BeF3-U7-RNA complex (PDB: 5LTA)15 was used as a template to generate a homology model using SWISS-MODEL15,16,17,18,19,20 (https://swissmodel.expasy.org/). This model was chosen as the template because it had the highest score in models complexed with RNA and adenosine triphosphate (ATP) in the local alignment using BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi) against the Protein Data Bank (PDB) database.21 Specific variants were made on the generated model using Chimera 1.1122 with the swapaa function. The single-stranded RNA motif and ADP-BeF3 of the 5LTA model was retained and used to view possible RNA and ATP contacts of the DHX37 pathogenic variants.
Annotations from UniProtKB (https://www.uniprot.org/uniprot/Q8IY37) and Pfam (http://pfam.xfam.org/protein/Q8IY37) were used as a guide to mark the domains in the structural model of DHX37. Some adjustments were made as compared with UniprotKB and Pfam based on the structurally defined domains of the DEAH-box family.23
Collection of human fetal gonads and human immunohistochemistry
Human fetal gonads were isolated from material available following elective surgical termination of pregnancy during the first trimester at the Department of Gynecology at Copenhagen University Hospital (Rigshospitalet) and Hvidovre Hospital, Denmark. The regional ethics committee approved this study (permit number H-1-2012-007) and women gave their informed written and oral consent. None of the terminations were for reasons of fetal abnormality and all fetuses appeared morphologically normal. The fetuses in this collection were between gestational week (GW) 7 and 12, with fetal age determined by scanning crown–rump length. Fetal testis tissue was isolated in ice-cold phosphate buffered saline (PBS) and immediately fixed in formalin. Immunohistochemistry was conducted as previously described with anti-DHX37 (HPA047607, Sigma/Prestige Antibodies) diluted 1:50 and antigen retrieval in TEG buffer (10 mM Tris, 0.5 mM EGTA, pH 9.0).24 Immunofluorescence was conducted as previously described,25 with anti-DHX37 (HPA047607, Sigma/Prestige Antibodies) diluted 1:200 and anti-OCT4 (sc-5279, Santa Cruz Biotechnology) diluted 1:100. Immunofluorescence on the human cell lines RT4, KGN, and HEK 293 was performed as described elsewhere10 using anti-DHX37 (HPA047607, Sigma/Prestige Antibodies) diluted 1:200.
Expression profiling in developing mouse gonads
For quantitative reverse-transcription PCR (qRT-PCR) of mouse tissue, messenger RNA (mRNA) was extracted from subdissected gonads of 6 XX and 6 XY 11.5 dpc mouse embryos using the RNeasy Plus Micro Kit (Qiagen). Each sample was then mixed with FastSYBR green master mix (Applied Biosystems) and either Dhx37 or Hrpt1 primers, plated in duplicate, and run on a 7500 Fast Real-Time PCR System (Applied Biosystems). Whole-mount in situ hybridization of 11.5 dpc wild-type (WT) XY gonads has been previously described.26 Immunofluorescence staining with anti-DHX37 (HPA047607, Sigma/Prestige Antibodies), anti-OCT4 (SC-5279, Santa Cruz Biotechnology), and DAPI (Vectashield with DAPI, Vector Laboratories) was performed on transverse sections of 11.5 dpc XY gonads. Sections were imaged at 20× using an LSM 700 Inverted Confocal Microscope (Zeiss).
DHX37 expression vectors containing the all six missense pathogenic variants were generated by site-directed mutagenesis (QuikChange, Stratagene) with the use of WT DHX37 complementary DNA (cDNA) in both pAC-GFP and pCMV6-Myc expression vectors as templates. The entire coding sequence of all mutant plasmids was confirmed by direct sequencing prior to functional studies. The pcDNA-SOX9-Flag vector was a gift from Francis Poulat (Institut de Génétique Moléculaire de Montpellier, France).
Single-cell array analysis of Nr5A1 +, XY somatic cells of the developing murine gonad
We analyzed public single-cell RNA-seq (scRNA-seq) data from Nr5A1+ cells of the developing XY murine gonad as described elsewhere.27 The data correspond to expression of transcript with fkpm >1 at single-cell level in the developing male murine gonad at specific time points in embryonic development (E10.5, E11.5, E12,5, E13.5, and E16.5). The data were compiled into a spreadsheet that was used to generate a box and whisker plot using BioVinci data visualization package. The summary statistics used to create the box and whisker plot included the median of the data, the lower and upper quartiles (25% and 75%), and the minimum and maximum values array analysis.
Cellular localization of both WT-DHX37 and DHX37 mutant proteins were assayed by transfecting the different plasmids into HEK 293-T cells with the use of FuGENE HD (E231A, Promega) in chamber slides (C7182, 8 wells, Nunc) as described elsewhere10 using green fluorescent protein (GFP) signal from the DHX37-GFP WT and mutants, as well as antifibrillarin antibody (ab4566, Abcam) diluted 1:200. Images were obtained with a Leica Microsystems DMI4000B microscope at 100× magnification.
Genetic analysis of 46,XY DSD reveals DHX37 pathogenic variants
A genetic screen of 145 46,XY individuals with DSD of unexplained etiology identified 13 individuals who harbored recurrent and de novo heterozygous missense pathogenic variants involving six different amino acids in the putative RNA helicase DHX37. Pathogenic variants were specifically identified in children with 46,XY gonadal dysgenesis (9/81, 11%) and 46,XY TRS (4/16, 25%) but not in boys with either severe penoscrotal hypospadias or anorchia (Table 1 and 2). All amino acid changes, with the exception of the p.G1030E and p.R308Q pathogenic variants, are absent from public databases. The p.G1030E substitution is a very rare variant with a minor allelic frequency (MAF) of 4.9 × 10−5 in individuals of European ancestry (ExAC database http://exac.broadinstitute.org/), whereas the p.R308Q is absent from the ExAC database but is reported in one individual by genomic sequencing in the gnomAD database (http://gnomad.broadinstitute.org/). Combining both data sets indicates that this pathogenic variant has a MAF of 6.7 × 10−6. Five of six pathogenic variants analyzed were absent from either parent and are therefore de novo. One pathogenic variant, p.T304M was maternally inherited and the mode of inheritance in the remaining seven children is unknown because DNA from the parents was not available for study. The presenting phenotypes of children carrying pathogenic DHX37 pathogenic variants exist on a spectrum ranging from phenotypic females to males with bilateral or unilateral cryptorchidism (Table 1). However, of note the majority of pathogenic variants were associated with the presence of Wolffian and absence of Müllerian structures suggesting residual Sertoli and Leydig cell function during early testis formation (Fig. 1). No gonadal tissue was present following examination for four of the children. In all 13 children there was no evidence of any other somatic anomalies. All pathogenic variants were confirmed by Sanger sequencing.
DHX37 is one the most highly conserved genes in the human genome and is intolerant to loss-of-function and missense variants in the general population.28 Fisher’s exact test (two-tailed) on the frequency of loss-of-function and missense variants observed in our 46,XY DSD cohort, compared with rare (MAF < 0.01%) missense variants in the DHX37 gene from 32,500 control individuals of matched-ancestry (ExAC database), shows a highly significant enrichment of rare missense variant in the DHX37 gene in the overall DSD cohort (P value = 5.8 × 10−10). The association with the subgroups of 46,XY gonadal dysgenesis and 46,XY TRS is even more striking (P value = 6 × 10−12). If we consider the five de novo missense pathogenic variants in DHX37 and compare this with the frequency of de novo missense DHX37 variants in 2278 control individuals (denovo-db.gs.washington.edu), the DSD cohort is highly enriched for de novo variants (P value = 1.5 × 10−5). This may indeed be an underestimation because the inheritance of the DHX37 pathogenic variant was unknown in 7/13 children. Furthermore, in the family of patient 5, the pathogenic variant was both de novo and absent from the unaffected 46,XY brother.
Interestingly, with one exception, all pathogenic variants are clustered within the functional RecA1 and RecA2 domains of the protein and involve amino acid residues that are highly conserved through to yeast (Fig. 2a and Supplemental Fig. 1). Consistent with this finding, all amino acid changes are considered to be highly damaging by multiple predictive software programs. Eleven of the 13 children have pathogenic variants specifically in four amino acid residues. Five children were mutated for the R308 residue and two children each for the T304, R334, and R674 residues respectively. None of the 13 children carrying pathogenic variantss in DHX37 carried pathogenic variants in other genes known to cause 46,XY DSD.
In silico conservation and modeling of DHX37 amino acid substitutions
RNA helicases are characterized by a highly conserved core domain of two tandem RecA-like domains (RecA1: ATP-binding DEAH-box helicase, RecA2: C-terminal helicase), which are connected by a flexible linker (Fig. 2a).29,30 Within these domains are 11 sequence motifs conserved throughout to yeast, which are involved in RNA substrate interaction, nucleoside triphosphate (NTP) binding and hydrolysis, and the coordination of unwinding activity. Four of the pathogenic variants fall within the motifs Ia, Va, and VI, which have been implicated in RNA binding, coordination of ATP binding and unwinding, and ATP binding and hydrolysis respectively (Fig. 2b). To predict the molecular consequences of the pathogenic variants we generated homology models of DHX37 using a crystal structure of the DEAH-box helicase Prp43 (PDB ID:5LTA) in an active state complexed with single-stranded U7-RNA and a nonhydrolyzable ATP analog (ATP-BeF3).15
The pathogenic variants p.R308Q, p.R334L are located at the DNA/RNA contact interface and provide an electrostatic environment to accommodate nucleic acids (Fig. 2a, c). These two arginines (R308 and R334) are highly conserved within the DEAH-box family and their counterparts in Prp43 interact with the RNA backbone.15 The recurrent p.R308Q pathogenic variant found within the conserved sugar-phosphate binding site, Ia, removes a positive charge and likely weakens this interaction.31 The p.R334L substitutions a hydrophobic leucine at conserved positions otherwise occupied by charged or polar amino acids with predicted detrimental effects on DNA/RNA-binding. The variants p.S626L and p.R674Q map to sequence motif Va or VI, respectively, which are both involved in ATP binding, hydrolysis, and cross-talk with the unwinding machinery (Fig. 2d). Serine 626 interacts with water and magnesium in the active site and arginine 674 forms electrostatic interactions with the γ-phosphate of ATP. The residue p.T304 of motif Ia is not directly involved in RNA binding but mediates intramolecular packing, which would be affected by the bulkier methionine side-chain introduced in the p.T304M pathogenic variant (Fig. 2e). Further evidence in favor of causality of these pathogenic variants is indicated by the analysis of seven missense variants reported in the gnomAD/ExAC databases that are present in low frequencies in the general population and may not be pathogenic (Table S2). These are located in the RecA1 and RecA2 domains. In silico modeling of all seven low frequency non-pathogenic variants indicated that in contrast to the pathogenic variants, they are predicted not to have either major structural or functional consequences (Supplemental data and Fig S2).
Expression analysis of DHX37 in early gonad development and functional studies
Consistent with a role in testis determination and early testis development, DHX37 is expressed exclusively in somatic cell lineages of the mouse and human gonad during testis determination and development (Fig. 3). The highest concentration of the protein is at the nuclear membrane, although protein is also observed in the cytoplasm and in the nucleolus of some cells (Fig. 3). Analysis of protein expression in different tissues from adults reveals that DHX37 is highly localized at the nuclear membrane in multiple human and mouse cell lines (https://www.proteinatlas.org/ENSG00000150990-DHX37/cell). Although expression was not observed in germ cells in fetal gonads, in adult human testes the protein is mainly localized in spermatogonia (Fig. S3; https://www.proteinatlas.org/ENSG00000150990-DHX37/tissue/testis#img). Single-cell expression analysis of Nr5a1+ somatic cells of the developing XY mouse gonad also indicates that Dhx37 is coexpressed with the sex-determining gene Sox9 in a proportion of cells (Fig. S4). When transfected into HEK 293 cells, the wild-type DHX37 protein and all six mutant proteins showed localization to the nucleolus (Fig. S5).
We provide compelling genetic evidence that specific variants in the DEAH-box protein DHX37, which encodes a putative RNA helicase, are a frequent cause of nonsyndromic 46,XY gonadal dysgenesis as well as TRS. The frequency of pathogenic variants associated with gonadal dysgenesis of 11% is similar to that described previously for each of the genes SRY, NR5A1, and MAP3K1.10 Where tested, all pathogenic variants are de novo with one exception, which was inherited from the phenotypically normal mother. This suggests that the penetrance of the variants is high and that the phenotype is sex-limited.
In contrast to the range of phenotypes associated with variants in other testis-determining genes, pathogenic variants involving DHX37 are associated with TRS but not anorchia. Children with TRS and with either female or ambiguous external genitalia are considered to have had a normal testis determination but have then lost testicular tissue at a critical period during the first 16 weeks of gestation. The genital phenotype may range predominantly from male to female, including marked sex ambiguity depending on the duration of normal testicular function prior to the loss of testicular tissue. Previously, a child with a pathogenic variant in the testis-determining factor NR5A1 (p.V355M) was reported, who presented with bilateral anorchia and reduced penile length; however, his dizygotic twin brother was also heterozygous for the change yet had normal development, suggesting that other genetic factors may be involved.32 Here, we found that 25% of children with clinically well-defined TRS carried pathogenic variants in the DHX37 gene. These data indicate that DHX37 has critical roles not only in early human testis determination but also in the maintenance of testicular tissue during an early phase of testis development. They also establish that 46,XY gonadal dysgenesis and TRS can be part of the same clinical spectrum with the same underlying genetic etiology.
The external genitalia of children carrying DHX37 pathogenic variants ranged from completely female to male with bilateral cryptorchidism. Four of the 13 children had virilized external genitalia and were raised as male suggesting that functional Leydig cells were present during fetal development. There is no evidence for a genotype/phenotype correlation. For example, five children carried the recurrent p.R308Q pathogenic variant with a phenotype that varied from female with primary amenorrhea to male with micropenis and bilateral cryptorchidism.
The yeast ortholog of DHX37, Dhr1, is required for ribosome biogenesis.33,34,35 Dhr1 is a essential component of the small subunit (SSU) processome, where its activity drives the transition of the SSU processome to pre-40S maturation pathway.35 Recently, the human DHX37 protein was also shown to be required for maturation of the small ribosomal subunit in the nucleolus of human HeLa cells by interacting with similar protein partners and small nucleolar RNAs suggesting that this function is conserved in eukaryotes.36
Two homozygous variants in DHX37 have been suggested to cause severe microcephaly, intellectual disability, and cortical atrophy in two unrelated individuals.37 However, both variants (p.R487H and p.N419K) are not located within known conserved and functional domains of RecA1 and RecA2. Although there was no statistical evidence in favor of pathogenicity, these pathogenic variants may have resulted in a severe congenital phenotype due to their homozygosity, location within the protein, and/or they may represent hypermorphic or neomorphic pathogenic variants. Further genetic investigations of this syndromic form of congenital microcephaly are required.
Disorders associated with ribosome biogenesis, the ribosomopathies, are an emerging and poorly understood branch of medicine.38,39 Indeed, three human ribosomopathies are caused by pathogenic variants in other components of the SSU processome: UTP4 (MIM 607456) pathogenic variants and North American Indian childhood cirrhosis (NAIC; MIM 604901); UTP14 (MIM 300508) with infertility, ovarian cancer, and scleroderma; and EMG1 (MIM 611531) with Bowen–Conradi syndrome (MIM 211180).38,39 The mechanism(s) of how a pathogenic variant in a widely expressed protein involved in a basic cellular function can generate a highly specific human phenotype are unknown. However, a zebrafish Dhx37 missense mutant has been reported in association with anomalies in the production of glycine receptor mRNAs, leading to an impact on neuron glycinergic synaptic transmission and altered behavior.40 This suggests that DHX37 may be involved in precursor mRNA (pre-mRNA) splicing with substrate specificity for certain transcripts at least in some cell lineages. These data raise the intriguing possibility that some forms of 46,XY DSD, caused by anomalies of early testis development, are also ribosomopathies.
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The authors thank Eszter Regős and Tamás Micsik, Semmelweis University, Budapest, Hungary and Ewa Rajpert-De Meyts, Rigshospitalet, Copenhagen, Denmark for valuable comments on the study. A.B. is funded in part by a research grant from the European Society of Pediatric Endocrinology, and by the Agence Nationale de la Recherche (ANR), ANR-10-LABX-73 REVIVE and ANR-17-CE14-0038-01. J.C.A. is a Wellcome Trust Senior Research Fellow in Clinical Science (grant 098513/Z/12/Z) with support from the National Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation Trust, University College London, and Great Ormond Street Hospital Children’s Charity. A.G. acknowledges support from the UK Medical Research Council through core funding at the Harwell Institute (MC_U142684167). RJ is supported by a Research Grants Council of Hong Kong General Research Fund (RGC/GRF) project number 17128918, a Health and Medical Research Fund (06174006) and Germany/Hong Kong Joint Research Scheme sponsored by the Research Grants Council of Hong Kong and the German Academic Exchange. This work is supported by the COST Action DSDnet BM130.
The authors declare no conflicts of interest.
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McElreavey, K., Jorgensen, A., Eozenou, C. et al. Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome. Genet Med (2019) doi:10.1038/s41436-019-0606-y
- disorders of sex development (DSD)
- testicular regression syndrome
- RNA helicase
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD
Journal of the Endocrine Society (2019)