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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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Kaydedildi:
Detaylı Bibliyografya
Yazar: D’Andrea, Alan D.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Online Erişim: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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