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Article

A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.

Behavioral and brain functions : BBF - 14 May 2011

Yu Jindan, He Xue, Yao Dan, Li Zhongyue, Li Hui, Zhao Zhengyan

Abstract excerpt

BACKGROUND: Synaptic genes, NLGN3 and NLGN4X, two homologous members of the neuroligin family, have been supposed as predisposition loci for autism spectrum disorders (ASDs), and defects of these two genes have been identified in a small fraction of individuals with ASDs. But no such rare variant in these two genes has as yet been adequately replicated in Chinese population and no common variant has been further...

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Identifiers

PMID: 21569590
DOI: 10.1186/1744-9081-7-13
PMCID: PMC3120659

Genes

NLGN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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