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Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2.
Ruskamo, Salla; Nieminen, Tuomo; Kristiansen, Cecilie K; Vatne, Guro H; Baumann, Anne; Hallin, Erik I; Raasakka, Arne; Joensuu, Päivi; Bergmann, Ulrich; Vattulainen, Ilpo; Kursula, Petri.
Afiliação
  • Ruskamo S; Faculty of Biochemistry and Molecular Medicine, University of Oulu, 90220, Oulu, Finland.
  • Nieminen T; Department of Physics, Tampere University of Technology, 33720, Tampere, Finland.
  • Kristiansen CK; Department of Biomedicine, University of Bergen, 5020, Bergen, Norway.
  • Vatne GH; Department of Biomedicine, University of Bergen, 5020, Bergen, Norway.
  • Baumann A; Department of Biomedicine, University of Bergen, 5020, Bergen, Norway.
  • Hallin EI; Division of Psychiatry, Haukeland University Hospital, 5021, Bergen, Norway.
  • Raasakka A; Department of Biomedicine, University of Bergen, 5020, Bergen, Norway.
  • Joensuu P; Department of Biomedicine, University of Bergen, 5020, Bergen, Norway.
  • Bergmann U; Department of Sustainable Chemistry, Technical Faculty, University of Oulu, 90570, Oulu, Finland.
  • Vattulainen I; Faculty of Biochemistry and Molecular Medicine, University of Oulu, 90220, Oulu, Finland.
  • Kursula P; Biocenter Oulu, University of Oulu, 90220, Oulu, Finland.
Sci Rep ; 7(1): 6510, 2017 07 26.
Article em En | MEDLINE | ID: mdl-28747762
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P2 de Mielina / Mutação de Sentido Incorreto Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Finlândia
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P2 de Mielina / Mutação de Sentido Incorreto Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Finlândia