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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Association Studies Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554198/
https://www.ncbi.nlm.nih.gov/pubmed/23148125
http://dx.doi.org/10.1093/hmg/dds476

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554198/
https://www.ncbi.nlm.nih.gov/pubmed/23148125
http://dx.doi.org/10.1093/hmg/dds476

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