ZMYND11

Publications

Oates St et al. ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clin Genet. 2021;100(4):412-429. PMID: 34216016.

Yates TM et al. ZMYND11ÔÇÉrelated syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. Hum mutat. 2020;41(5):1042-1050. PMID: 32097528.

Guo R et al. BS69/ZMYND11 reads and connects histone H3.3 lysine 36 trimethylation-decorated chromatin to regulated pre-mRNA processing. Mol Cell. 2014 Oct 23;56(2):298-310. PMID: 25263594