Mutations of the SLX4 gene in Fanconi anemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng.750.pdf
Reference26 articles.
1. Auerbach, A.D. Fanconi anemia and its diagnosis. Mutat. Res. 668, 4–10 (2009).
2. Auerbach, A.D. & Wolman, S.R. Susceptibility of Fanconi′s anaemia fibroblasts to chromosome damage by carcinogens. Nature 261, 494–496 (1976).
3. Moldovan, G.L. & D'Andrea, A.D. How the fanconi anemia pathway guards the genome. Annu. Rev. Genet. 43, 223–249 (2009).
4. Knipscheer, P. et al. The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science 326, 1698–1701 (2009).
5. Fekairi, S. et al. Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases. Cell 138, 78–89 (2009).
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