Associated Papers
ZMYND11 Restrains KMT2A to Enable a Neuronal Developmental Program.
Greben AW et al.
Biorxiv : the Preprint Server for Biology, 2025
41279818 (PubMed )
Supplement: media-1.pdf
Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modeling.
Tordai C et al.
Schizophrenia Research, 2024
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum.
Yates TM et al.
Human Mutation, 2020
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