Basilicata FM et al. De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nat Genet. 2018;50(10):1442-1451. PMID: 30224647.
Brunet T et al. Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder. Genet Med. 2021;23(2):384-395. PMID: 33173220.
MSL3