Rare CNVs and Tag SNPs at 15q11.2 Are Associated With Schizophrenia in the Han Chinese Population

BACKGROUND: Rare copy number variations (CNVs) were involved in the etiology of neuropsychiatric disorders, and some of them appeared to be shared risk factors for several different diseases. One of those promising loci is the CNV at 15q11.2, including 4 genes, TUBGCP5, CYFIP1, NIPA2, and NIPA1. Sev...

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Dettagli Bibliografici
Autori principali: Zhao, Qian, Li, Tao, Zhao, XinZhi, Huang, Ke, Wang, Ti, Li, ZhiQiang, Ji, Jue, Zeng, Zhen, Zhang, Zhao, Li, Kan, Feng, GuoYin, St Clair, David, He, Lin, Shi, YongYong
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2013
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Regular Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3627771/
https://ncbi.nlm.nih.gov/pubmed/22317777
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbr197
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