Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
Sjursen W; Haukanes BI; Grindedal EM; Aarset H; Stormorken A; Engebretsen LF; Jonsrud C; Bjørnevoll I; Andresen PA; Ariansen S; Lavik LA; Gilde B; Bowitz-Lothe IM; Maehle L; Møller P; Journal Of Medical Genetics, 2010, vol. 47, issue 9, p 579, ISSN 14686244. ISBN 14686244.

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