Detection of a novel mutation in exon 20 of the BRCA1 gene

Hereditary breast cancer constitutes 5–10% of all breast cancer cases. Inherited mutations in the BRCA1 and BRCA2 tumor-suppressor genes account for the majority of hereditary breast cancer cases. The BRCA1 C-terminal region (BRCT) has a functional duplicated globular domain, which helps with DNA da...

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Detalles Bibliográficos
Autores principales: Chakraborty, Abhijit, Katarkar, Atul, Chaudhuri, Keya, Mukhopadhyay, Ashis, Basak, Jayasri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2013
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275959/
https://www.ncbi.nlm.nih.gov/pubmed/24297685
http://dx.doi.org/10.2478/s11658-013-0110-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275959/
https://www.ncbi.nlm.nih.gov/pubmed/24297685
http://dx.doi.org/10.2478/s11658-013-0110-3

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