Associated Papers
Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder.
Brunet T et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM10_ESM.xlsx › Supplementary_Data_8
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation.
Basilicata MF et al.
Nature Genetics, 2018
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