Identification of a BRCA2 mutation in a Turkish family with early‐onset breast cancer

We used a multi‐gene panel testing to identify the germline variants in a mother‐daughter pair with early‐onset breast cancer, and detected one pathogenic protein‐truncating variant in BRCA2. Our results highlight the importance of genetic testing in identifying the pathogenic mutation running in ca...

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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: Celik, Elifnaz, Ermis Tekkus, Kubra, Akcay, Izzet Mehmet, Alkurt Sal, Gizem, Ezberci, Fikret, Dinler Doganay, Gizem, Doganay, Levent
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6132100/
https://ncbi.nlm.nih.gov/pubmed/30214756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1625
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