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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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| Vydáno v: | Oncotarget |
|---|---|
| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Impact Journals LLC
2019
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| Témata: | |
| On-line přístup: | 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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