Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

Ayers, Katie L.; Eggers, Stefanie; Rollo, Ben N.; Smith, Katherine R.; Davidson, Nadia M.; Siddall, Nicole A.; Zhao, Liang; Bowles, Josephine; Weiss, Karin; Zanni, Ginevra; Burglen, Lydie; Ben-Shachar, Shay; Rosensaft, Jenny; Raas-Rothschild, Annick; Jørgensen, Anne; Schittenhelm, Ralf B.; Huang, Cheng; Robevska, Gorjana; van den Bergen, Jocelyn; Casagranda, Franca; Cyza, Justyna; Pachernegg, Svenja; Wright, David K.; Bahlo, Melanie; Oshlack, Alicia; O’Brien, Terrence J.; Kwan, Patrick; Koopman, Peter; Hime, Gary R.; Girard, Nadine; Hoffmann, Chen; Shilon, Yuval; Zung, Amnon; Bertini, Enrico; Milh, Mathieu; Ben Rhouma, Bochra; Belguith, Neila; Bashamboo, Anu; McElreavey, Kenneth; Banne, Ehud; Weintrob, Naomi; BenZeev, Bruria; Sinclair, Andrew H.

doi:10.1038/s41467-023-39372-x

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Published: 15 June 2023

Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

Katie L. Ayers ORCID: orcid.org/0000-0002-6840-3186^1,2,
Stefanie Eggers³,
Ben N. Rollo⁴,
Katherine R. Smith⁵,
Nadia M. Davidson^5,6,7,
Nicole A. Siddall ORCID: orcid.org/0000-0002-0144-8400⁸,
Liang Zhao ORCID: orcid.org/0000-0002-3489-7421⁹,
Josephine Bowles ORCID: orcid.org/0000-0003-2867-7438^9,10,
Karin Weiss¹¹,
Ginevra Zanni ORCID: orcid.org/0000-0002-6367-1843¹²,
Lydie Burglen ORCID: orcid.org/0000-0002-1119-6809^13,14,
Shay Ben-Shachar¹⁵,
Jenny Rosensaft¹⁶,
Annick Raas-Rothschild^17,18,
Anne Jørgensen¹⁹,
Ralf B. Schittenhelm ORCID: orcid.org/0000-0001-8738-1878²⁰,
Cheng Huang ORCID: orcid.org/0000-0002-4575-1233²⁰,
Gorjana Robevska¹,
Jocelyn van den Bergen¹,
Franca Casagranda⁸,
Justyna Cyza¹,
Svenja Pachernegg^1,2,
David K. Wright⁴,
Melanie Bahlo⁵^nAff36,
Alicia Oshlack ORCID: orcid.org/0000-0001-9788-5690^21,22,
Terrence J. O’Brien^4,23,
Patrick Kwan^4,23,
Peter Koopman⁹,
Gary R. Hime ORCID: orcid.org/0000-0003-4732-3184⁸,
Nadine Girard ORCID: orcid.org/0000-0001-8639-9275²⁴,
Chen Hoffmann²⁵,
Yuval Shilon²⁶,
Amnon Zung^27,28,
Enrico Bertini¹²,
Mathieu Milh ORCID: orcid.org/0000-0002-2454-8543²⁴,
Bochra Ben Rhouma^29,30,
Neila Belguith^30,31,
Anu Bashamboo³²,
Kenneth McElreavey³²,
Ehud Banne^16,33,
Naomi Weintrob^18,34,
Bruria BenZeev³⁵ &
…
Andrew H. Sinclair ORCID: orcid.org/0000-0003-2741-7992^1,2

Nature Communications volume 14, Article number: 3566 (2023) Cite this article

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The Original Article was published on 09 June 2023

Correction to: Nature Communications https://doi.org/10.1038/s41467-023-39040-0, published online 09 June 2023

In this article, the author name Kenneth McElreavey was incorrectly written as Kenneth MacElreavey.

The original article has been corrected.

Author information

Melanie Bahlo
Present address: Department of Medical Biology, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, Australia

Authors and Affiliations

The Murdoch Children’s Research Institute, Melbourne, VIC, Australia
Katie L. Ayers, Gorjana Robevska, Jocelyn van den Bergen, Justyna Cyza, Svenja Pachernegg & Andrew H. Sinclair
Department of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia
Katie L. Ayers, Svenja Pachernegg & Andrew H. Sinclair
The Victorian Clinical Genetics Services, Melbourne, VIC, Australia
Stefanie Eggers
Department of Neuroscience, Central Clinical School, Monash University, Alfred Centre, Melbourne, VIC, Australia
Ben N. Rollo, David K. Wright, Terrence J. O’Brien & Patrick Kwan
Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia
Katherine R. Smith, Nadia M. Davidson & Melanie Bahlo
School of BioSciences, Faculty of Science, University of Melbourne, Melbourne, VIC, Australia
Nadia M. Davidson
Department of Medical Biology, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, VIC, Australia
Nadia M. Davidson
Department of Anatomy and Physiology, The University of Melbourne, Melbourne, VIC, Australia
Nicole A. Siddall, Franca Casagranda & Gary R. Hime
Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia
Liang Zhao, Josephine Bowles & Peter Koopman
School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, Australia
Josephine Bowles
Genetics Institute, Rambam Health Care Campus, Rappaport Faculty of Medicine, Institute of Technology, Haifa, Israel
Karin Weiss
Unit of Muscular and Neurodegenerative Disorders and Unit of Developmental Neurology, Department of Neurosciences, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
Ginevra Zanni & Enrico Bertini
Centre de Référence des Malformations et Maladies Congénitales du Cervelet, Et Laboratoire de Neurogénétique Moléculaire, Département de Génétique et Embryologie Médicale, APHP. Sorbonne Université, Hôpital Trousseau, Paris, France
Lydie Burglen
Developmental Brain Disorders Laboratory, Imagine Institute, INSERM UMR 1163, Paris, France
Lydie Burglen
Genetic Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel
Shay Ben-Shachar
Genetics Institute, Kaplan Medical Center, Hebrew University Hadassah Medical School, Rehovot, 76100, Israel
Jenny Rosensaft & Ehud Banne
Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat Gan, Israel
Annick Raas-Rothschild
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Annick Raas-Rothschild & Naomi Weintrob
Department of Growth and Reproduction, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Anne Jørgensen
Monash Proteomics and Metabolomics Facility, Biomedicine Discovery Institute, Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia
Ralf B. Schittenhelm & Cheng Huang
The Peter MacCallum Cancer Centre, Melbourne, VIC, Australia
Alicia Oshlack
School of Mathematics and Statistics, The University of Melbourne, Melbourne, VIC, Australia
Alicia Oshlack
Department of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Melbourne, VIC, Australia
Terrence J. O’Brien & Patrick Kwan
Department of Pediatric Neurology, Aix-Marseille Université, APHM, Timone Hospital, Marseille, France
Nadine Girard & Mathieu Milh
Radiology Department, Sheba medical Centre, Tel Aviv, Israel
Chen Hoffmann
Kaplan Medical Center, Hebrew University Hadassah Medical School, Rehovot, 76100, Israel
Yuval Shilon
Pediatrics Department, Kaplan Medical Center, Rehovot, 76100, Israel
Amnon Zung
Faculty of Medicine, Hebrew University of Jerusalem, Hadassah Medical School, Jerusalem, Israel
Amnon Zung
Higher Institute of Nursing Sciences of Gabes, University of Gabes, Gabes, Tunisia
Bochra Ben Rhouma
Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, Sfax University, Sfax, Tunisia
Bochra Ben Rhouma & Neila Belguith
Department of Congenital and Hereditary Diseases, Charles Nicolle Hospital, Tunis, Tunisia
Neila Belguith
Institut Pasteur, Université de Paris, CNRS UMR3738, Human Developmental Genetics, 75015, Paris, France
Anu Bashamboo & Kenneth McElreavey
The Rina Mor Genetic Institute, Wolfson Medical Center, Holon, 58100, Israel
Ehud Banne
Pediatric Endocrinology Unit, Dana-Dwek Children’s Hospital, Tel Aviv Medical Center, Tel Aviv, Israel
Naomi Weintrob
Sheba Medical Center, Tel Aviv, Israel
Bruria BenZeev

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Katie L. Ayers
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Stefanie Eggers
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Ben N. Rollo
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Katherine R. Smith
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Liang Zhao
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Josephine Bowles
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Karin Weiss
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Melanie Bahlo
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Anu Bashamboo
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Naomi Weintrob
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Bruria BenZeev
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Andrew H. Sinclair
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Correspondence to Katie L. Ayers.

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Ayers, K.L., Eggers, S., Rollo, B.N. et al. Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects. Nat Commun 14, 3566 (2023). https://doi.org/10.1038/s41467-023-39372-x

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Published: 15 June 2023
DOI: https://doi.org/10.1038/s41467-023-39372-x

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Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

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