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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2013
विषय:
Association Studies Articles
ऑनलाइन पहुंच: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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