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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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Dades bibliogràfiques
Publicat a:Oncotarget
Autors principals: Yoshida, Reiko, Watanabe, Chie, Yokoyama, Shiro, Inuzuka, Mayuko, Yotsumoto, Junko, Arai, Masami, Nakamura, Seigo
Format: Artigo
Idioma:Inglês
Publicat: Impact Journals LLC 2019
Matèries:
Accés en línia: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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