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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Oncotarget
Päätekijät: Yoshida, Reiko, Watanabe, Chie, Yokoyama, Shiro, Inuzuka, Mayuko, Yotsumoto, Junko, Arai, Masami, Nakamura, Seigo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Impact Journals LLC 2019
Aiheet:
Linkit: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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