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Identification of a BRCA2 mutation in a Turkish family with early‐onset breast cancer
We used a multi‐gene panel testing to identify the germline variants in a mother‐daughter pair with early‐onset breast cancer, and detected one pathogenic protein‐truncating variant in BRCA2. Our results highlight the importance of genetic testing in identifying the pathogenic mutation running in ca...
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| Veröffentlicht in: | Clin Case Rep |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6132100/ https://ncbi.nlm.nih.gov/pubmed/30214756 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1625 |
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