Classifications within Molecular Subtypes Enables Identification of BRCA1/BRCA2 Mutation Carriers by RNA Tumor Profiling

Pathogenic germline mutations in BRCA1 or BRCA2 are detected in less than one third of families with a strong history of breast cancer. It is therefore expected that mutations still remain undetected by currently used screening methods. In addition, a growing number of BRCA1/2 sequence variants of u...

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Detalles Bibliográficos
Autores principales: Larsen, Martin J., Kruse, Torben A., Tan, Qihua, Lænkholm, Anne-Vibeke, Bak, Martin, Lykkesfeldt, Anne E., Sørensen, Kristina P., Hansen, Thomas v. O., Ejlertsen, Bent, Gerdes, Anne-Marie, Thomassen, Mads
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660328/
https://www.ncbi.nlm.nih.gov/pubmed/23704984
http://dx.doi.org/10.1371/journal.pone.0064268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660328/
https://www.ncbi.nlm.nih.gov/pubmed/23704984
http://dx.doi.org/10.1371/journal.pone.0064268

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