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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515604/
https://www.ncbi.nlm.nih.gov/pubmed/23227193
http://dx.doi.org/10.1371/journal.pone.0050640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515604/
https://www.ncbi.nlm.nih.gov/pubmed/23227193
http://dx.doi.org/10.1371/journal.pone.0050640

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