Analysis of Copy Number Variation in Alzheimer’s Disease: the NIA-LOAD/NCRAD Family Study

Copy number variants (CNVs) are DNA regions that have gains (duplications) or losses (deletions) of genetic material. CNVs may encompass a single gene or multiple genes and can affect their function. They are hypothesized to play an important role in certain diseases. We previously examined the role...

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Hoofdauteurs: Swaminathan, Shanker, Shen, Li, Kim, Sungeun, Inlow, Mark, West, John D., Faber, Kelley M., Foroud, Tatiana, Mayeux, Richard, Saykin, Andrew J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2012
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3500615/
https://ncbi.nlm.nih.gov/pubmed/22486522
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