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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. (2016)

First Author: Singh T

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