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

Rahner, N.; Brockschmidt, F.F.; Steinke, V.; Kahl, P.; Becker, T.; Vasen, H.F.A.; ... ; Dutch Canc Genetics Grp (2012)

Article / Letter to editor

• Association study
• ESR
• HNPCC
• KAT2A
• Lynch syndrome
• MAX
• Mutation analysis
• PCNA

• All authors: Rahner, N.; Brockschmidt, F.F.; Steinke, V.; Kahl, P.; Becker, T.; Vasen, H.F.A.; Wijnen, J.T.; 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
• Date: 2012-03-31
• Journal: Familial Cancer
• Volume: 11
• Issue: 1
• Pages: 19 - 26
• DOI: doi:10.1007/s10689-011-9489-z