DNA repair genes implicated in triple negative familial non-BRCA1/2 breast cancer predisposition

Among breast cancers, 10 to 15% of cases would be due to hereditary risk. In these familial cases, mutations in BRCA1 and BRCA2 are found in only 15% to 20%, meaning that new susceptibility genes remain to be found. Triple-negative breast cancers represent 15% of all breast cancers, and are generall...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Am J Cancer Res
Egile Nagusiak: Ollier, Marie, Radosevic-Robin, Nina, Kwiatkowski, Fabrice, Ponelle, Flora, Viala, Sandrine, Privat, Maud, Uhrhammer, Nancy, Bernard-Gallon, Dominique, Penault-Llorca, Frédérique, Bignon, Yves-Jean, Bidet, Yannick
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: e-Century Publishing Corporation 2015
Gaiak:
Original Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4548324/
https://ncbi.nlm.nih.gov/pubmed/26328243
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