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Genomic and phenotypic analysis of BRCA2 mutated breast cancers reveals co-occurring changes linked to progression
BACKGROUND: Inherited mutations in the BRCA2 gene greatly increase the risk of developing breast cancer. Consistent with an important role for BRCA2 in error-free DNA repair, complex genomic changes are frequently observed in tumors derived from BRCA2 mutation carriers. Here, we explore the impact o...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3262207/ https://ncbi.nlm.nih.gov/pubmed/21958427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/bcr3020 |
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