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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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Enregistré dans:
Détails bibliographiques
Auteur principal: D’Andrea, Alan D.
Format: Artigo
Langue:Inglês
Publié: 2013
Sujets:
Accès en ligne: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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