A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

We assessed the role of rare copy number variants (CNVs) in Alzheimer's disease (AD) using intensity data from 3260 AD cases and 1290 age-matched controls from the genome-wide association study (GWAS) conducted by the Genetic and Environmental Risk for Alzheimer's disease Consortium (GERAD...

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Detalhes bibliográficos
Main Authors: Chapman, Jade, Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, Paul, Stretton, Alexandra, Holmans, Peter, Owen, Michael J., O'Donovan, Michael C., Williams, Julie, Kirov, George
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
Assuntos:
Association Studies Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3554198/
https://ncbi.nlm.nih.gov/pubmed/23148125
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds476
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