Association of PALB2 sequence variants with the risk of familial and early-onset breast cancer in a South-American population

BACKGROUND: Germline mutations in PALB2 have been identified in approximately 1% of familial breast cancer (BC) in several populations. Nevertheless its contribution in the South-American population is unknown. The goal of this study was to determine the prevalence of PALB2 mutations in the Chilean...

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Detalhes bibliográficos
Publicado no:BMC Cancer
Main Authors: Leyton, Yessica, Gonzalez-Hormazabal, Patricio, Blanco, Rafael, Bravo, Teresa, Fernandez-Ramires, Ricardo, Morales, Sebastian, Landeros, Natalia, Reyes, Jose M, Peralta, Octavio, Tapia, Julio C, Gomez, Fernando, Waugh, Enrique, Ibañez, Gladys, Pakomio, Janara, Grau, Gilberto, Jara, Lilian
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4323211/
https://ncbi.nlm.nih.gov/pubmed/25636233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-015-1033-3
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