ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. (2021)
Attributed to:
The role of chromatin remodelling factors in cerebellar development and autism
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.14023
PubMed Identifier: 34216016
Publication URI: http://europepmc.org/abstract/MED/34216016
Type: Journal Article/Review
Volume: 100
Parent Publication: Clinical genetics
Issue: 4
ISSN: 0009-9163