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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Bibliografski detalji
Glavni autori: Swaminathan, Shanker, Huentelman, Matthew J., Corneveaux, Jason J., Myers, Amanda J., Faber, Kelley M., Foroud, Tatiana, Mayeux, Richard, Shen, Li, Kim, Sungeun, Turk, Mari, Hardy, John, Reiman, Eric M., Saykin, Andrew J.
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2012
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3515604/
https://ncbi.nlm.nih.gov/pubmed/23227193
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0050640
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