Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case–control study

BACKGROUND: The p16-Leiden founder mutation in the CDKN2A gene is the most common cause of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome in the Netherlands. Individuals with this mutation are at increased risk for developing melanoma of the skin, as well as pancreatic cancer. However, th...

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Detalles Bibliográficos
Autores principales: Potjer, Thomas P, van der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, van den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, van der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480449/
https://www.ncbi.nlm.nih.gov/pubmed/26111702
http://dx.doi.org/10.1186/s13104-015-1235-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480449/
https://www.ncbi.nlm.nih.gov/pubmed/26111702
http://dx.doi.org/10.1186/s13104-015-1235-4

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