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Functional analysis of HNPCC-related missense mutations in MSH2.
Lützen A, de Wind N, Georgijevic D, Nielsen FC, Rasmussen LJ. Lützen A, et al. Among authors: georgijevic d. Mutat Res. 2008 Oct 14;645(1-2):44-55. doi: 10.1016/j.mrfmmm.2008.08.015. Epub 2008 Sep 4. Mutat Res. 2008. PMID: 18822302