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

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...

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Detalles Bibliográficos
Autores principales: Yu, Jindan, He, Xue, Yao, Dan, Li, Zhongyue, Li, Hui, Zhao, Zhengyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120659/
https://www.ncbi.nlm.nih.gov/pubmed/21569590
http://dx.doi.org/10.1186/1744-9081-7-13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120659/
https://www.ncbi.nlm.nih.gov/pubmed/21569590
http://dx.doi.org/10.1186/1744-9081-7-13

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