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Genetic variation in the 22q11 locus and susceptibility to schizophrenia

An increased prevalence of microdeletions at the 22q11 locus has been reported in samples of patients with schizophrenia. 22q11 microdeletions represent the highest known genetic risk factor for the development of schizophrenia, second only to that of the monozygotic cotwin of an affected individual...

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Detaylı Bibliyografya
Yayımlandı:Proc Natl Acad Sci U S A
Asıl Yazarlar: Liu, Hui, Abecasis, Gonçalo R., Heath, Simon C., Knowles, Alyson, Demars, Sandra, Chen, Ying-Jiun, Roos, J. Louw, Rapoport, Judith L., Gogos, Joseph A., Karayiorgou, Maria
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2002
Konular:
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC139234/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12477929/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.232186099
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