Publication
Characterization of a novel founderMSH6mutation causing Lynch syndrome in the French Canadian population
A novelMSH6founder mutation in Quebec
E. Castellsagué, J. Liu, A. Volenik, S. Giroux, R. Gagné, B. Maranda, A. Roussel-Jobin, J. Latreille, R. Laframboise, L. Palma, L. Kasprzak, V.A. Marcus, M. Breguet, S. Nolet, Z. El-Haffaf, K. Australie, A. Gologan, O. Aleynikova, K. Oros-Klein, C. Greenwood, A.M. Mes-Masson, D. Provencher, M. Tischkowitz, G. Chong, F. Rousseau, W.D. Foulkes
Clinical Genetics, November 2014, Wiley
DOI: 10.1111/cge.12526