A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

E. van Riel, M.G.E.M. Ausems, F.B.L. Hogervorst, I Kluijt, M.E. van Gijn, J. van Echtelt, K. Scheidel-Jacobse, E.F.A.M. Hennekam, R.P. Stulp, Y.J. Vos, G.J.A. Offerhaus, F.H. Menko, J.J.P. Gille

Research output: Contribution to journalArticleAcademicpeer-review

49 Downloads (Pure)
Original languageUndefined/Unknown
Pages (from-to)7
JournalHereditary Cancer in Clinical Practice
Publication statusPublished - 2010

Cite this