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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Detalles Bibliográficos
Autores principales: Yoshida, Reiko, Watanabe, Chie, Yokoyama, Shiro, Inuzuka, Mayuko, Yotsumoto, Junko, Arai, Masami, Nakamura, Seigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524931/
https://www.ncbi.nlm.nih.gov/pubmed/31143373
http://dx.doi.org/10.18632/oncotarget.26852

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524931/
https://www.ncbi.nlm.nih.gov/pubmed/31143373
http://dx.doi.org/10.18632/oncotarget.26852

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