Common alleles contribute to schizophrenia in CNV carriers

The genetic architecture of schizophrenia is complex, involving risk alleles ranging from common alleles of weak effect to rare alleles of large effect, the best exemplar of the latter being large copy number variants (CNVs). It is currently unknown whether pathophysiology in those with defined rare...

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Detaylı Bibliyografya
Yayımlandı:Mol Psychiatry
Asıl Yazarlar: Tansey, K E, Rees, E, Linden, D E, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, P, Kirov, G, Walters, J, Owen, M J, O'Donovan, M C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2016
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4960448/
https://ncbi.nlm.nih.gov/pubmed/26390827
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2015.143
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