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CHCHD10 mutations and motor neuron disease: the distribution in Finnish patients.
Penttilä, Sini; Jokela, Manu; Saukkonen, Anna Maija; Toivanen, Jari; Palmio, Johanna; Lähdesmäki, Janne; Sandell, Satu; Shcherbii, Mariia; Auranen, Mari; Ylikallio, Emil; Tyynismaa, Henna; Udd, Bjarne.
Afiliação
  • Penttilä S; Neuromuscular Research Center, Tampere University and University Hospital, Tampere, Finland.
  • Jokela M; Division of Clinical Neurosciences, Turku University Hospital and University of Turku, Turku, Finland.
  • Saukkonen AM; Department of Neurology, Central Hospital of Northern Karelia, Joensuu, Finland.
  • Toivanen J; Department of Neurology, Central Hospital of Northern Karelia, Joensuu, Finland.
  • Palmio J; Neuromuscular Research Center, Tampere University and University Hospital, Tampere, Finland.
  • Lähdesmäki J; Division of Clinical Neurosciences, Turku University Hospital and University of Turku, Turku, Finland.
  • Sandell S; Department of Neurology, Seinäjoki Central Hospital, Seinäjoki, Finland.
  • Shcherbii M; Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
  • Auranen M; Department of Clinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
  • Ylikallio E; Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
  • Tyynismaa H; Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
  • Udd B; Neuromuscular Research Center, Tampere University and University Hospital, Tampere, Finland.
J Neurol Neurosurg Psychiatry ; 88(3): 272-277, 2017 03.
Article em En | MEDLINE | ID: mdl-27810918
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Paraplegia Espástica Hereditária / Miopatias Mitocondriais / Proteínas Mitocondriais / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Atrofia Muscular Espinal / Paraplegia Espástica Hereditária / Miopatias Mitocondriais / Proteínas Mitocondriais / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article