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A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
Rydning, S L; Wedding, I M; Koht, J; Chawla, M; Øye, A-M; Sheng, Y; Vigeland, M D; Selmer, K K; Tallaksen, C M E.
Afiliación
  • Rydning SL; Department of Neurology, Oslo University Hospital, Norway.
  • Wedding IM; Institute of Clinical Medicine, University of Oslo, Norway.
  • Koht J; Department of Neurology, Oslo University Hospital, Norway.
  • Chawla M; Institute of Clinical Medicine, University of Oslo, Norway.
  • Øye AM; Department of Neurology, Drammen Hospital, Vestre Viken Health Trust, Norway.
  • Sheng Y; Department of Radiology and Nuclear Medicine, Oslo University Hospital, Norway.
  • Vigeland MD; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Norway.
  • Selmer KK; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Norway.
  • Tallaksen CM; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Norway.
Eur J Neurol ; 23(4): 763-71, 2016 Apr.
Article en En | MEDLINE | ID: mdl-26756429
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía / Metaloendopeptidasas / Paraplejía Espástica Hereditaria Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Humans País/Región como asunto: Europa Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Noruega
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía / Metaloendopeptidasas / Paraplejía Espástica Hereditaria Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Humans País/Región como asunto: Europa Idioma: En Revista: Eur J Neurol Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Noruega