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GCH1 mutations in hereditary spastic paraplegia.
Varghaei, Parizad; Yoon, Grace; Estiar, Mehrdad A; Veyron, Simon; Leveille, Etienne; Dupré, Nicolas; Trempe, Jean-François; Rouleau, Guy A; Gan-Or, Ziv.
Afiliação
  • Varghaei P; Division of Experimental Medicine, Department of Medicine, McGill University, Montreal, Quebec, Canada.
  • Yoon G; Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
  • Estiar MA; Divisions of Neurology and Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Canada.
  • Veyron S; Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
  • Leveille E; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
  • Dupré N; Department of Pharmacology & Therapeutics and Centre de Recherche en Biologie Structurale - FRQS, McGill University, Montréal, Canada.
  • Trempe JF; Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
  • Rouleau GA; Axe Neurosciences, CHU de Québec-Université Laval, Quebec City, Québec, Canada.
  • Gan-Or Z; Department of Medicine, Faculty of Medicine, Université Laval, Quebec City, Quebec, Canada.
Clin Genet ; 100(1): 51-58, 2021 07.
Article em En | MEDLINE | ID: mdl-33713342
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / GTP Cicloidrolase / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / GTP Cicloidrolase / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article