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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...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Frontiers Media S.A.
2014
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| Gaiak: | |
| Sarrera elektronikoa: | 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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