Functional characterization of MLH1 missense variants identified in lynch syndrome patients

Author(s):
Andersen, S.D.; Liberti, S.E.; Lutzen, A.; Drost, M.; Bernstein, I.; Nilbert, M.; Dominguez, M.; Nystrom, M.; Hansen, T.V.; Christoffersen, J.W.; Jager, A.C.; Wind, N. de (0000-0002-3143-5061); Nielsen, F.C.; Torring, P.M.; Rasmussen, L.J.
Published
2012
Publication type
Article / Letter to editor
Lynch syndromemismatch repairfunctional assayMLH1
Date issued
2012-12-31
Language
English
Is part of
Human Mutation (2012), Vol. 33, no. 12, p. 1647-1655
hdl
1887/97794
doi
10.1002/humu.22153