Article
BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases.
Journal of ovarian research - 2 May 2020
Suszynska Malwina, Ratajska Magdalena, Kozlowski Piotr
Abstract excerpt
BACKGROUND: It is estimated that more than 20% of ovarian cancer cases are associated with a genetic predisposition that is only partially explained by germline mutations in the BRCA1 and BRCA2 genes. Recently, several pieces of evidence showed that mutations in three genes involved in the homologous recombination DNA repair pathway, i.e., BRIP1, RAD51C, and RAD51D, are associated with a high risk of ovarian...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
