FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population

PURPOSE: The FANCM c.5101C>T nonsense mutation was previously found to associate with breast cancer in the Finnish population, especially among triple-negative cases. Here, we studied the prevalence of three other FANCM variants: c.5791C>T, which has been reported to predispose to familial bre...

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Detalles Bibliográficos
Autores principales: Kiiski, Johanna I., Tervasmäki, Anna, Pelttari, Liisa M., Khan, Sofia, Mantere, Tuomo, Pylkäs, Katri, Mannermaa, Arto, Tengström, Maria, Kvist, Anders, Borg, Åke, Kosma, Veli-Matti, Kallioniemi, Anne, Schleutker, Johanna, Bützow, Ralf, Blomqvist, Carl, Aittomäki, Kristiina, Winqvist, Robert, Nevanlinna, Heli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Epidemiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645429/
https://www.ncbi.nlm.nih.gov/pubmed/28702895
http://dx.doi.org/10.1007/s10549-017-4388-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645429/
https://www.ncbi.nlm.nih.gov/pubmed/28702895
http://dx.doi.org/10.1007/s10549-017-4388-0

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