Mutation analysis of BRCA1/2 mutations with special reference to polymorphic SNPs in Indian breast cancer patients

BACKGROUND: Germline mutations BRCA1 and BRCA2 contribute almost equally in the causation of breast cancer (BC). The type of mutations in the Indian population that cause this condition is largely unknown. PURPOSE: In this cohort, 79 randomized BC patients were screened for various types of BRCA1 an...

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Detalles Bibliográficos
Autores principales: Shah, Nidhi D, Shah, Parth S, Panchal, Yash Y, Katudia, Kalpesh H, Khatri, Nikunj B, Ray, Hari Shankar P, Bhatiya, Upti R, Shah, Sandip C, Shah, Bhavini S, Rao, Mandava V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953318/
https://www.ncbi.nlm.nih.gov/pubmed/29785135
http://dx.doi.org/10.2147/TACG.S155955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5953318/
https://www.ncbi.nlm.nih.gov/pubmed/29785135
http://dx.doi.org/10.2147/TACG.S155955

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