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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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| Autors principals: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2013
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| Matèries: | |
| Accés en línia: | 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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