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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Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 2007
Témata:
Biological Sciences
On-line přístup: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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