Characteristics of breast cancer patients tested for germline BRCA1/2 mutations by next‐generation sequencing in Ramathibodi Hospital, Mahidol University

INTRODUCTION: Germline mutations in BRCA1/2 are the most common cause of hereditary breast and ovarian cancer (HBOC) syndrome. Few studies published during the past decade reported the prevalence of germline BRCA mutations in Asian patients with breast cancer. We aimed to assess the prevalence and c...

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Detalles Bibliográficos
Autores principales: Oranratnachai, Songporn, Yamkaew, Watchalawalee, Tunteeratum, Atchara, Sukarayothin, Thongchai, Iemwimangsa, Nareenart, Panvichien, Ravat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875646/
https://www.ncbi.nlm.nih.gov/pubmed/35778884
http://dx.doi.org/10.1002/cnr2.1664

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875646/
https://www.ncbi.nlm.nih.gov/pubmed/35778884
http://dx.doi.org/10.1002/cnr2.1664

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