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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Bibliographic Details
Published in:Oncotarget
Main Authors: Yoshida, Reiko, Watanabe, Chie, Yokoyama, Shiro, Inuzuka, Mayuko, Yotsumoto, Junko, Arai, Masami, Nakamura, Seigo
Format: Artigo
Language:Inglês
Published: Impact Journals LLC 2019
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Research Paper
Online Access: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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