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BRCA1: A Missing Link in the Fanconi Anemia/BRCA Pathway
Domchek et al provide a case report of a 28 year-old woman with congenital abnormalities, inherited ovarian cancer, and carboplatin hypersensitivity. Interestingly, the woman has validated germline mutations in both BRCA1 alleles. These findings further implicate BRCA1 in the Fanconi Anemia/BRCA pat...
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2013
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3693462/ https://ncbi.nlm.nih.gov/pubmed/23580280 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/2159-8290.CD-13-0044 |
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