Loss of function germline mutations in RAD51D in women with ovarian carcinoma

OBJECTIVE: RAD51D, a gene in the Fanconi Anemia-BRCA homologous recombination pathway, has recently been shown to harbor germline mutations responsible for ovarian carcinoma in multiply affected families. We aimed to extend these results to ovarian carcinoma in the general population. METHODS: We se...

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Detalhes bibliográficos
Main Authors: Wickramanayake, Anneka, Bernier, Greta, Pennil, Christopher, Casadei, Silvia, Agnew, Kathy J, Stray, Sunday M., Mandell, Jessica, Garcia, Rochelle L., Walsh, Tom, King, Mary-Claire, Swisher, Elizabeth M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3905744/
https://ncbi.nlm.nih.gov/pubmed/22986143
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ygyno.2012.09.009
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