Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. (2016)
Attributed to:
Molecular Genetic Studies of Schizophrenia
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/nn.4267
PubMed Identifier: 26974950
Publication URI: http://europepmc.org/abstract/MED/26974950
Type: Journal Article/Review
Volume: 19
Parent Publication: Nature neuroscience
Issue: 4
ISSN: 1097-6256