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Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families
BACKGROUND: BRCA1 and BRCA2 mutations explain approximately one-fifth of the inherited susceptibility in high-risk Finnish hereditary breast and ovarian cancer (HBOC) families. EMSY is located in the breast cancer-associated chromosomal region 11q13. The EMSY gene encodes a BRCA2-interacting protein...
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| Veröffentlicht in: | BMC Cancer |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5525221/ https://ncbi.nlm.nih.gov/pubmed/28738860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-017-3488-x |
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