Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. (2023)

First Author: Lin JR
Attributed to:  MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41380-023-02009-y

PubMed Identifier: 36869225

Publication URI: http://europepmc.org/abstract/MED/36869225

Type: Journal Article/Review

Volume: 28

Parent Publication: Molecular psychiatry

Issue: 5

ISSN: 1359-4184