Melançon, Serge B.
Montreal Children's Hospital · McGill University
2 papers on CoChat
Most cited papers
- Verified
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF
Engert, J. C., Bérubé, P., Mercier, J., Doré, C., Lepage, P., Ge, B., Bouchard, J.-P., Mathieu, J., Melançon, S. B., Schalling, M., et al. (2000) · Nature Genetics
Genetic Neurodegenerative DiseasesHereditary Neurological Disorders
Cited by 434
- Verified
Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec
Larochelle, J., Alvarez, F., Bussières, J.-F., Chevalier, I., Dallaire, L., Dubois, J., Faucher, F., Fenyves, D., Goodyer, P., Grenier, A., et al. (2012) · Molecular Genetics and Metabolism
Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism
Cited by 137
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