Analysis of Heterozygous BRCA1 5382ins Founder Mutation in a Cohort of Egyptian Breast Cancer Female Patients Using Pyrosequencing Technique

BACKGROUND: Up to half of the heritable mutations in breast cancer (BC) are attributed to BRCA1 and BRCA2 genes. The mutation prevalence is variable based on ethnicity and may be influenced by founder mutations. The aim of this pilot study is to determine for the first time, the prevalence of BRCA1...

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Detalles Bibliográficos
Autores principales: Mogahed, Salwa H Gomaa, Hamed, Yasser S, Moursy, Yassmin E Ibrahim, Saied, Marwa H Mahomoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332123/
https://www.ncbi.nlm.nih.gov/pubmed/32102521
http://dx.doi.org/10.31557/APJCP.2020.21.2.431

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332123/
https://www.ncbi.nlm.nih.gov/pubmed/32102521
http://dx.doi.org/10.31557/APJCP.2020.21.2.431

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