Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1

Germline mutations that inactivate BRCA1 are responsible for breast and ovarian cancer susceptibility. One possible outcome of genetic testing for BRCA1 is the finding of a genetic variant of uncertain significance for which there is no information regarding its cancer association. This outcome lead...

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Detalhes bibliográficos
Main Authors: Carvalho, Marcelo, Pino, Maria A., Karchin, Rachel, Beddor, Jennifer, Godinho-Netto, Martha, Mesquita, Rafael D., Rodarte, Renato S., Vaz, Danielle C., Monteiro, Viviane A., Manoukian, Siranoush, Colombo, Mara, Ripamonti, Carla B., Rosenquist, Richard, Suthers, Graeme, Borg, Ake, Radice, Paolo, Grist, Scott A., Monteiro, Alvaro N.A., Billack, Blase
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2682550/
https://ncbi.nlm.nih.gov/pubmed/18992264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mrfmmm.2008.09.017
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