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Triple A syndrome presenting as complicated hereditary spastic paraplegia.
Leveille, Etienne; Gonorazky, Hernan D; Rioux, Marie-France; Hazrati, Lili-Naz; Ruskey, Jennifer A; Carnevale, Amanda; Spiegelman, Dan; Dionne-Laporte, Alexandre; Rouleau, Guy A; Yoon, Grace; Gan-Or, Ziv.
Afiliación
  • Leveille E; Faculty of Medicine, McGill University, Montréal, Québec, Canada.
  • Gonorazky HD; Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Rioux MF; Department of Neurology, Université de Sherbrooke, Sherbrooke, Québec, Canada.
  • Hazrati LN; Department of Laboratory Medicine and Pathobiology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Ruskey JA; Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
  • Carnevale A; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
  • Spiegelman D; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Dionne-Laporte A; Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
  • Rouleau GA; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
  • Yoon G; Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
  • Gan-Or Z; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
Mol Genet Genomic Med ; 6(6): 1134-1139, 2018 11.
Article en En | MEDLINE | ID: mdl-30381913
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Paraplejía Espástica Hereditaria / Proteínas de Complejo Poro Nuclear / Proteínas del Tejido Nervioso Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2018 Tipo del documento: Article País de afiliación: Canadá
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Paraplejía Espástica Hereditaria / Proteínas de Complejo Poro Nuclear / Proteínas del Tejido Nervioso Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2018 Tipo del documento: Article País de afiliación: Canadá