A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population

BACKGROUND: Recent research has implicated that mutations in the neurexin-1 (NRXN1) gene on chromosome 2p16.3 might play a role in schizophrenia, autism, and nicotine dependence. In order to explore the association of NRXN1 polymorphisms with schizophrenia, we made a case-control association study i...

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Detalhes bibliográficos
Main Authors: Yue, Weihua, Yang, Yongfeng, Zhang, Yanling, Lu, Tianlan, Hu, Xiaofeng, Wang, Lifang, Ruan, Yanyan, Lv, Luxian, Zhang, Dai
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3080281/
https://ncbi.nlm.nih.gov/pubmed/21477380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-7-7
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