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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
BACKGROUND: Single-nucleotide polymorphisms (SNPs) in genes involved in DNA repair are good candidates to be tested as phenotypic modifiers for carriers of mutations in the high-risk susceptibility genes BRCA1 and BRCA2. The base excision repair (BER) pathway could be particularly interesting given...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
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Nature Publishing Group
2011
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3078599/ https://ncbi.nlm.nih.gov/pubmed/21427728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bjc.2011.91 |
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