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Analysis of clinical characteristics of breast cancer patients with the Japanese founder mutation BRCA1 L63X

Background: BRCA1 and BRCA2 are high-penetrance inherited genes; different founder mutations have been reported in various areas and races. By using trial registration data from the Japanese hereditary breast and ovarian cancer syndrome (HBOC) consortium, we aimed to explore the clinicopathological...

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Detalhes bibliográficos
Publicado no:Oncotarget
Main Authors: Yoshida, Reiko, Watanabe, Chie, Yokoyama, Shiro, Inuzuka, Mayuko, Yotsumoto, Junko, Arai, Masami, Nakamura, Seigo
Formato: Artigo
Idioma:Inglês
Publicado em: Impact Journals LLC 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6524931/
https://ncbi.nlm.nih.gov/pubmed/31143373
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.26852
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