Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome

So far 18 MLH3 germline mutations/variants have been identified in familial colorectal cancer cases. Sixteen of these variants are amino acid substitutions of which the pathogenic nature is still unclear. These substitutions are known as unclassified variants or UVs. To clarify a possible role for e...

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Veröffentlicht in:Genes chromosomes & cancer 2009-04, Vol.48 (4), p.340-350
Hauptverfasser: Ou, Jianghua, Rasmussen, Merete, Westers, Helga, Andersen, Sofie D., Jager, Paul O., Kooi, Krista A., Niessen, Renée C., Eggen, Bart J. L., Nielsen, Finn C., Kleibeuker, Jan H., Sijmons, Rolf H., Rasmussen, Lene J., Hofstra, Robert M. W.
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Sprache:eng
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