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Article

Human GRIN2B variants in neurodevelopmental disorders.

Journal of pharmacological sciences - 1 Oct 2016

Hu Chun, Chen Wenjuan, Myers Scott J, Yuan Hongjie, Traynelis Stephen F

Abstract excerpt

The development of whole exome/genome sequencing technologies has given rise to an unprecedented volume of data linking patient genomic variability to brain disorder phenotypes. A surprising number of variants have been found in the N-methyl-d-aspartate receptor (NMDAR) gene family, with the GRIN2B gene encoding the GluN2B subunit being implicated in many cases of neurodevelopmental disorders, which are...

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Identifiers

PMID: 27818011
DOI: 10.1016/j.jphs.2016.10.002
PMCID: PMC5125235

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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