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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Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2013
Sujets:
Association Studies Articles
Accès en ligne: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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