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Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2 transcripts
BACKGROUND: Genetic screening of breast cancer patients and their families have identified a number of variants of unknown clinical significance in the breast cancer susceptibility genes, BRCA1 and BRCA2. Evaluation of such unclassified variants may be assisted by web-based bioinformatic prediction...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
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BioMed Central
2010
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2897790/ https://ncbi.nlm.nih.gov/pubmed/20507642 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-80 |
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