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Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population

E Castellsagué1, J Liu, A Volenik

  • 1Department of Human Genetics, McGill University, Montreal, Quebec, Canada; Department of Medical Genetics, The Lady Davis Institute, Segal Cancer Centre, Jewish General Hospital, Montreal, Quebec, Canada; Translational Research Laboratory, Catalan Institute of Oncology, Bellvitge Institute for Biomedical Research, Barcelona, Spain.

Clinical Genetics
|October 17, 2014
PubMed

Keywords:
French CanadiansLynch syndromeMSH6colorectal cancerendometrial cancerfounder mutationsmolecular diagnostics

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