Persistent URL of this record https://hdl.handle.net/1887/97794
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Functional characterization of MLH1 missense variants identified in lynch syndrome patients
- All authors
- 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; Nielsen, F.C.; Torring, P.M.; Rasmussen, L.J.
- Date
- 2012-12-31
- Journal
- Human Mutation
- Volume
- 33
- Issue
- 12
- Pages
- 1647 - 1655