Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

Author(s):
Rahner, N.; Brockschmidt, F.F.; Steinke, V.; Kahl, P.; Becker, T.; Vasen, H.F.A.; Wijnen, J.T. (0000-0003-2805-6922); Tops, C.J.M.; Holinski-Feder, E.; Ligtenberg, M.J.L.; Spruijt, L.; Gorgens, H.; Stemmler, S.; Kloor, M.; Dietmaier, W.; Schumacher, J.; Nothen, M.M.; Propping, P.; Dutch Canc Genetics Grp
Published
2012
Publication type
Article / Letter to editor
Association studyESRHNPCCKAT2ALynch syndromeMAXMutation analysisPCNA
Date issued
2012-03-31
Language
English
Is part of
Familial Cancer (2012), Vol. 11, no. 1, p. 19-26
hdl
1887/100231
doi
10.1007/s10689-011-9489-z