A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants

Author(s):
Drost, M.; Zonneveld, J.B.; Hees, S. van; Rasmussen, L.J.; Hofstra, R.M.W.; Wind, N. de (0000-0002-3143-5061)
Published
2012
Publication type
Article / Letter to editor
Lynch syndromeDNA mismatch repairvariants of uncertain significancefunctional assayMSH2MSH6
Date issued
2012-03-31
Language
English
Is part of
Human Mutation (2012), Vol. 33, no. 3, p. 488-494
hdl
1887/99237