Cargando…
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...
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: | |
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 |
Ejemplares similares
-
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome
por: Kiiski, Johanna I., et al.
Publicado: (2016) -
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
por: Mantere, Tuomo, et al.
Publicado: (2017) -
Recurrent moderate‐risk mutations in Finnish breast and ovarian cancer patients
por: Nurmi, Anna, et al.
Publicado: (2019) -
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor
por: Cannon‐Albright, Lisa A., et al.
Publicado: (2020) -
Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls
por: Behravan, Hamid, et al.
Publicado: (2018)