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Article

Association of genetic variants of GRIN2B with autism.

Scientific reports - 6 Feb 2015

Pan Yongcheng, Chen Jingjing, Guo Hui, Ou Jianjun, Peng Yu, Liu Qiong, Shen Yidong, Shi Lijuan, Liu Yalan, Xiong Zhimin, Zhu Tengfei, Luo Sanchuan, Hu Zhengmao, Zhao Jingping, Xia Kun

Abstract excerpt

Autism (MIM 209850) is a complex neurodevelopmental disorder characterized by social communication impairments and restricted repetitive behaviors. It has a high heritability, although much remains unclear. To evaluate genetic variants of GRIN2B in autism etiology, we performed a system association study of common and rare variants of GRIN2B and autism in cohorts from a Chinese population, involving a total...

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Identifiers

PMID: 25656819
DOI: 10.1038/srep08296
PMCID: PMC4319152

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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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