Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas

BRCA1 and BRCA2 mutations are responsible for hereditary breast and ovarian cancer, but they also confer an increased risk for the development of rarer cancers associated with this syndrome, namely, cancer of the pancreas, male breast, peritoneum, and fallopian tube. The objective of this work was t...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:PLoS One
Autori principali: Pinto, Pedro, Peixoto, Ana, Santos, Catarina, Rocha, Patrícia, Pinto, Carla, Pinheiro, Manuela, Leça, Luís, Martins, Ana Teresa, Ferreira, Verónica, Bartosch, Carla, Teixeira, Manuel R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2016
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4988637/
https://ncbi.nlm.nih.gov/pubmed/27532258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0161438
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi