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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

Abstract 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 h...

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Bibliografiske detaljer
Principais autores: Malwina Suszynska, Magdalena Ratajska, Piotr Kozlowski
Format: Artigo
Sprog:Inglês
Udgivet: BMC 2020-05-01
Serier:Journal of Ovarian Research
Fag:
Online adgang:http://link.springer.com/article/10.1186/s13048-020-00654-3
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