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About this Biochemistry, Genetics and Molecular Biology article

Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population by Castellsagué, E.; Liu, J.; Volenik, A.; Giroux, S.; Gagné, R.; Maranda, B.; Roussel-Jobin, A.; Latreille, J.; Laframboise, R.; Palma, L.; Kasprzak, L.; Marcus, V.A.; Breguet, M.; Nolet, S.; El-Haffaf, Z.; Australie, K.; Gologan, A.; Aleynikova, O.; Oros-Klein, K.; Greenwood, C.; Mes-Masson, A.M.; Provencher, D.; Tischkowitz, M.; Chong, G.; Rousseau, F.; Foulkes, W.D. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Castellsagué, E.; Liu, J.; Volenik, A.; Giroux, S.; Gagné, R.; Maranda, B.; Roussel-Jobin, A.; Latreille, J.; Laframboise, R.; Palma, L.; Kasprzak, L.; Marcus, V.A.; Breguet, M.; Nolet, S.; El-Haffaf, Z.; Australie, K.; Gologan, A.; Aleynikova, O.; Oros-Klein, K.; Greenwood, C.; Mes-Masson, A.M.; Provencher, D.; Tischkowitz, M.; Chong, G.; Rousseau, F.; Foulkes, W.D.
Publisher
John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
Published
2015
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)