GCH1 mutations in hereditary spastic paraplegia.

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第一作者： Parizad,Varghaei

第一单位： Division of Experimental Medicine, Department of Medicine, McGill University, Montreal, Quebec, Canada.;Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.

作者： Parizad,Varghaei ^[1] ; Grace,Yoon ^[2] ; Mehrdad A,Estiar ^[3] ; Simon,Veyron ^[4] ; Etienne,Leveille ^[5] ; Nicolas,Dupré ^[6] ; Jean-François,Trempe ^[4] ; Guy A,Rouleau ^[7] ; Ziv,Gan-Or ^[7]

作者单位： Division of Experimental Medicine, Department of Medicine, McGill University, Montreal, Quebec, Canada.;Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada. ^[1] Divisions of Neurology and Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Canada. ^[2] Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.;Department of Human Genetics, McGill University, Montreal, Quebec, Canada. ^[3] Department of Pharmacology & Therapeutics and Centre de Recherche en Biologie Structurale - FRQS, McGill University, Montréal, Canada. ^[4] Faculty of Medicine, McGill University, Montreal, Quebec, Canada. ^[5] Axe Neurosciences, CHU de Québec-Université Laval, Quebec City, Québec, Canada.;Department of Medicine, Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada. ^[6] Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.;Department of Human Genetics, McGill University, Montreal, Quebec, Canada.;Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada. ^[7]

关键词 GCH1 HSP dystonia spastic paraplegia