Analysis of PALB2/FANCN-associated breast cancer families

No more than ≈30% of hereditary breast cancer has been accounted for by mutations in known genes. Most of these genes, such as BRCA1, BRCA2, TP53, CHEK2, ATM, and FANCJ/BRIP1, function in DNA repair, raising the possibility that germ line mutations in other genes that contribute to this process also...

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Detalhes bibliográficos
Main Authors: Tischkowitz, Marc, Xia, Bing, Sabbaghian, Nelly, Reis-Filho, Jorge S., Hamel, Nancy, Li, Guilan, van Beers, Erik H., Li, Lili, Khalil, Tayma, Quenneville, Louise A., Omeroglu, Atilla, Poll, Aletta, Lepage, Pierre, Wong, Nora, Nederlof, Petra M., Ashworth, Alan, Tonin, Patricia N., Narod, Steven A., Livingston, David M., Foulkes, William D.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2007
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1871863/
https://ncbi.nlm.nih.gov/pubmed/17420451
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0701724104
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