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A novel germline BRCA1 mutation identified in a family with hereditary breast and ovarian cancer syndrome
Pathogenic germline mutations occurring in the BRCA1 (MIM:113705) and BRCA2 (MIM: 600185), which always result in truncated protein or nonsense-mediated mRNA decay, have been identified to increase the risk of hereditary breast, ovarian, pancreatic, prostate, and melanoma cancers. Recent studies sho...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Clin Med Insights Oncol |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
SAGE Publications
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8255550/ https://ncbi.nlm.nih.gov/pubmed/34276234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/11795549211028569 |
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