Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.

Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletions) genetic material. They may overlap genes affecting their function and have been shown to be associated with disease. We previously investigated the role of CNVs in late-onset Alzheimer's dise...

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Auteurs principaux: Shanker Swaminathan, Matthew J Huentelman, Jason J Corneveaux, Amanda J Myers, Kelley M Faber, Tatiana Foroud, Richard Mayeux, Li Shen, Sungeun Kim, Mari Turk, John Hardy, Eric M Reiman, Andrew J Saykin, Alzheimer's Disease Neuroimaging Initiative and NIA-LOAD/NCRAD Family Study Group
Format: article
Langue:EN
Publié: Public Library of Science (PLoS) 2012
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Accès en ligne:https://doaj.org/article/3c5684af656b4abeb7c5e3c3fea08753
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