Characterization of BRCA1/2 mutations in patients with family history of breast cancer in Armenia

Background. Breast cancer is one of the most common cancers in women worldwide. The germline mutations of the BRCA1 and BRCA2 genes are the most significant and well characterized genetic risk factors for hereditary breast cancer. Intensive research in the last decades has demonstrated that the inci...

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Detalles Bibliográficos
Autores principales: Atshemyan, Sofi, Chavushyan, Andranik, Berberian, Nerses, Sahakyan, Arthur, Zakharyan, Roksana, Arakelyan, Arsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357036/
https://www.ncbi.nlm.nih.gov/pubmed/28357044
http://dx.doi.org/10.12688/f1000research.10434.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357036/
https://www.ncbi.nlm.nih.gov/pubmed/28357044
http://dx.doi.org/10.12688/f1000research.10434.1

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