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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Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2012
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Research Article
Accesso online: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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