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Editorial

. 2016 Sep 1;73(9):1056-8.

doi: 10.1001/jamaneurol.2016.2095.

The Puzzle of Huntington Disease Phenocopies

Nicolas Dupré¹, Guy Rouleau²

Affiliations

Affiliations

¹ Faculty of Medicine, Laval University, Quebec City, Quebec, Canada2Clinic of Neuromuscular and Neurogenetic Diseases, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
² Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.

PMID: 27399805
DOI: 10.1001/jamaneurol.2016.2095

Editorial

The Puzzle of Huntington Disease Phenocopies

Nicolas Dupré et al. JAMA Neurol. 2016.

. 2016 Sep 1;73(9):1056-8.

doi: 10.1001/jamaneurol.2016.2095.

Authors

Nicolas Dupré¹, Guy Rouleau²

Affiliations

¹ Faculty of Medicine, Laval University, Quebec City, Quebec, Canada2Clinic of Neuromuscular and Neurogenetic Diseases, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
² Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.

PMID: 27399805
DOI: 10.1001/jamaneurol.2016.2095

No abstract available

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Comment on

Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
Mariani LL, Tesson C, Charles P, Cazeneuve C, Hahn V, Youssov K, Freeman L, Grabli D, Roze E, Noël S, Peuvion JN, Bachoud-Levi AC, Brice A, Stevanin G, Durr A. Mariani LL, et al. JAMA Neurol. 2016 Sep 1;73(9):1105-14. doi: 10.1001/jamaneurol.2016.2215. JAMA Neurol. 2016. PMID: 27400454

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