Investigation of germline variants in Bahraini women with breast cancer using next-generation sequencing based-multigene panel

Germline variants in BRCA1 and BRCA2 (BRCA1/2) genes are the most common cause of hereditary breast cancer. However, a significant number of cases are not linked to these two genes and additional high-, moderate- and low-penetrance genes have been identified in breast cancer. The advent of next-gene...

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Detalles Bibliográficos
Autores principales: Al-Kafaji, Ghada, Jassim, Ghufran, AlHajeri, Amani, Alawadhi, Amna Mohamed Tayeb, Fida, Mariam, Sahin, Ibrahim, Alali, Faisal, Fadel, Elias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473515/
https://www.ncbi.nlm.nih.gov/pubmed/37656691
http://dx.doi.org/10.1371/journal.pone.0291015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473515/
https://www.ncbi.nlm.nih.gov/pubmed/37656691
http://dx.doi.org/10.1371/journal.pone.0291015

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