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BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype
We have investigated the clinical significance of the BRCA1 variant p.His1673del in 14 families from the Emilia-Romagna region of Italy, including 20 breast and 23 ovarian cancer cases; four families displayed site-specific ovarian cancer. The variant, absent in human variation databases, has been r...
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| Publicado no: | Oncotarget |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Impact Journals LLC
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5410251/ https://ncbi.nlm.nih.gov/pubmed/28186987 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.15151 |
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