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Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families
BACKGROUND: Genes that, when mutated, cause Fanconi anemia or greatly increase breast cancer risk encode for proteins that converge on a homology-directed DNA damage repair process. Mutations in the SLX4 gene, which encodes for a scaffold protein involved in the repair of interstrand cross-links, ha...
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| Hauptverfasser: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2012
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3315397/ https://ncbi.nlm.nih.gov/pubmed/22401137 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2407-12-84 |
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