Published July 1, 2018
| Version Accepted Version
Journal article
Open
TheGBAp.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies
Authors/Creators
- 1. Montreal Neurological Institute; McGill University; Montréal Quebec Canada
- 2. Department of Epidemiology, Biostatistics and Occupational Health; McGill University; Montréal Quebec Canada
- 3. Department of Hematology; Jewish General Hospital, McGill University; Montréal Quebec Canada
- 4. Axe neurosciences du CHU de Québec; Université Laval; Québec Canada
- 5. Faculty of Medicine; McGill University; Montréal Quebec Canada
- 6. McGill Parkinson Program and Neurodegenerative Diseases Group, Montreal Neurological Institute; McGill University; Montréal Quebec Canada
- 7. Department of Pharmacology & Therapeutics; McGill University; Montréal Quebec Canada
- 8. Division of Neurology, Department of Medicine; University of Toronto; Toronto Ontario Canada
- 9. Department of Neurology; McGill University, Montreal General Hospital; Montreal Québec Canada
- 10. Hematology/Oncology; Centre Hospitalier Universitaire Sainte-Justine; Montréal Quebec Canada
- 11. Mark Freedman and Judy Jacobs Program for Gaucher Disease; Sinai Health System and University of Toronto; Toronto Ontario Canada
Description
This is the peer reviewed version of the following article: [Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.-A., Alam, A., Roncière, L., Spiegelman, D., Fon, E.A., Trempe, J.-F., Kalia, L.V., et al. (2018). TheGBAp.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies. Clinical Genetics 94, 339–345.], which has been published in final form at https://doi.org/10.1111/cge.13405. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
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