Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk

Although family history is a risk factor for pancreatic adenocarcinoma, much of the genetic etiology of this disease remains unknown. While genome-wide association studies have identified some common single nucleotide polymorphisms (SNPs) associated with pancreatic cancer risk, these SNPs do not exp...

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Bibliografiska uppgifter
Huvudupphovsmän: Willis, Jason A., Mukherjee, Semanti, Orlow, Irene, Viale, Agnes, Offit, Kenneth, Kurtz, Robert C., Olson, Sara H., Klein, Robert J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2014
Ämnen:
Genetics
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3923159/
https://ncbi.nlm.nih.gov/pubmed/24592275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00029
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