Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)

INTRODUCTION: Mutations in BRCA1 and BRCA2 confer a high risk of breast cancer (BC), but the magnitude of this risk seems to vary according to the study and various factors. Although controversial, there are data to support the hypothesis of allelic risk heterogeneity. METHODS: We assessed variation...

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Detalles Bibliográficos
Autores principales: Lecarpentier, Julie, Noguès, Catherine, Mouret-Fourme, Emmanuelle, Gauthier-Villars, Marion, Lasset, Christine, Fricker, Jean-Pierre, Caron, Olivier, Stoppa-Lyonnet, Dominique, Berthet, Pascaline, Faivre, Laurence, Bonadona, Valérie, Buecher, Bruno, Coupier, Isabelle, Gladieff, Laurence, Gesta, Paul, Eisinger, François, Frénay, Marc, Luporsi, Elisabeth, Lortholary, Alain, Colas, Chrystelle, Dugast, Catherine, Longy, Michel, Pujol, Pascal, Tinat, Julie, Lidereau, Rosette, Andrieu, Nadine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3680948/
https://www.ncbi.nlm.nih.gov/pubmed/22762150
http://dx.doi.org/10.1186/bcr3218

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3680948/
https://www.ncbi.nlm.nih.gov/pubmed/22762150
http://dx.doi.org/10.1186/bcr3218

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