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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Bibliografiske detaljer
Main Authors: 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
Sprog:Inglês
Udgivet: Public Library of Science 2012
Fag:
Research Article
Online adgang: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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