📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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

First Author: Singh T

Attributed to: Methylomic profiling in schizophrenia: towards an integrated genetic-epigenetic approach 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