Founder BRCA1 mutations in Nepalese population

BACKGROUND: Founder mutation is a heritable genetic alteration observed with high frequency in a geographically and culturally isolated population where one or more ancestors becomes the forebearer of the altered gene. The current study reports two founder mutations in the BRCA1 gene in the Nepalese...

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Detalles Bibliográficos
Autores principales: Mehta, Anurag, Diwan, Himanshi, Gupta, Garima, Nathany, Shrinidhi, Agnihotri, Shalini, Dhanda, Surender
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pathologists/The Korean Society for Cytopathology 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288895/
https://www.ncbi.nlm.nih.gov/pubmed/35698740
http://dx.doi.org/10.4132/jptm.2022.05.02

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288895/
https://www.ncbi.nlm.nih.gov/pubmed/35698740
http://dx.doi.org/10.4132/jptm.2022.05.02

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