BRCA1: a missing link in the Fanconi anemia/BRCA pathway.

Abstract:

:Domchek and colleagues provide a case report of a 28-year-old woman with congenital abnormalities, inherited ovarian cancer, and carboplatin hypersensitivity. Interestingly, the woman had validated germline mutations in both BRCA1 alleles. These findings further implicate BRCA1 in the Fanconi anemia/BRCA pathway and have important implications for BRCA1 genetic testing.

journal_name

Cancer Discov

journal_title

Cancer discovery

authors

D'Andrea AD

doi

10.1158/2159-8290.CD-13-0044

subject

Has Abstract

pub_date

2013-04-01 00:00:00

pages

376-8

issue

4

eissn

2159-8274

issn

2159-8290

pii

3/4/376

journal_volume

3

pub_type

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