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Whole-genome detection of disease-associated deletions or excess homozygosity in a case–control study of rheumatoid arthritis

Unlike genome-wide association studies, few comprehensive studies of copy number variation's contribution to complex human disease susceptibility have been performed. Copy number variations are abundant in humans and represent one of the least well-studied classes of genetic variants; in additi...

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Detalhes bibliográficos
Main Authors: Wu, Chih-Chieh, Shete, Sanjay, Jo, Eun-Ji, Xu, Yaji, Lu, Emily Y., Chen, Wei V., Amos, Christopher I.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3578409/
https://ncbi.nlm.nih.gov/pubmed/23223014
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds512
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