Fig. 1 | European Journal of Human Genetics

Fig. 1

From: A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy

Fig. 1

NAA10 variants a NAA10 variants identified to date in patients with global development delays and/or intellectual disabilities. Variants found in female patients are shown as red circles; variants identified in male patients as red squares. Heterozygous females with no or very mild phenotypes reported are shown as white circles with a black dot. b Pedigrees for family 1 and family 2 presented in this study

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