Cargando…
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women
BACKGROUND: PALB2 has recently been identified as a breast cancer susceptibility gene. PALB2 mutations are rare causes of hereditary breast cancer but may be important in countries such as Finland where a founder mutation is present. We sought to estimate the contribution of PALB2 mutations to the b...
Autores principales: | Foulkes, William D, Ghadirian, Parviz, Akbari, Mohammed Reza, Hamel, Nancy, Giroux, Sylvie, Sabbaghian, Nelly, Darnel, Andrew, Royer, Robert, Poll, Aletta, Fafard, Eve, Robidoux, André, Martin, Ginette, Bismar, Tarek A, Tischkowitz, Marc, Rousseau, Francois, Narod, Steven A |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2246183/ https://www.ncbi.nlm.nih.gov/pubmed/18053174 http://dx.doi.org/10.1186/bcr1828 |
Ejemplares similares
-
Weight History, Smoking, Physical Activity and Breast Cancer Risk among French-Canadian Women Non-Carriers of More Frequent BRCA1/2 Mutations
por: Bissonauth, Vishnee, et al.
Publicado: (2009) -
RAD51C germline mutations in breast and ovarian cancer patients
por: Akbari, Mohammad R, et al.
Publicado: (2010) -
Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada
por: Hartley, Taila, et al.
Publicado: (2014) -
Contribution of the PALB2 c.2323C>T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent
por: Tischkowitz, Marc, et al.
Publicado: (2013) -
A PALB2 mutation associated with high risk of breast cancer
por: Southey, Melissa C, et al.
Publicado: (2010)