Management Strategies of Breast Cancer Patients with BRCA1 and BRCA2 Pathogenic Germline Variants

Most of breast cancer cases are sporadic; however, 15–20% are associated with family history, and some are inherited. Among those, deleterious mutations in BRCA1 and BRCA2 tumor suppressor genes are the most commonly encountered pathogenic germline variants (PGVs). Given the availability and afforda...

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Detalles Bibliográficos
Autores principales: Edaily, Sarah, Abdel-Razeq, Hikmat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343017/
https://www.ncbi.nlm.nih.gov/pubmed/35923470
http://dx.doi.org/10.2147/OTT.S369844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343017/
https://www.ncbi.nlm.nih.gov/pubmed/35923470
http://dx.doi.org/10.2147/OTT.S369844

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