Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families

Fanconi anemia is a genetically heterogeneous autosomal recessive disorder characterized by development abnormalities, bone marrow failure, and childhood cancers. Compelling evidence indicates a common genetic basis for FA and breast/ovarian cancer susceptibility. Recently, biallelic germ-line mutat...

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Detalhes bibliográficos
Main Authors: de Garibay, Gorka Ruiz, Díaz, Avellaneda, Gaviña, Belén, Romero, Atocha, Garre, Pilar, Vega, Ana, Blanco, Ana, Tosar, Alicia, Díez, Orland, Pérez-Segura, Pedro, Díaz-Rubio, Eduardo, Caldés, Trinidad, de la Hoya, Miguel
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2013
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3722678/
https://ncbi.nlm.nih.gov/pubmed/23211700
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.268
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