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SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.
Osmanovic, Alma; Widjaja, Maylin; Förster, Alisa; Weder, Julia; Wattjes, Mike P; Lange, Inken; Sarikidi, Anastasia; Auber, Bernd; Raab, Peter; Christians, Anne; Preller, Matthias; Petri, Susanne; Weber, Ruthild G.
Afiliação
  • Osmanovic A; Department of Human Genetics, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
  • Widjaja M; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Förster A; Department of Human Genetics, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
  • Weder J; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Wattjes MP; Department of Human Genetics, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
  • Lange I; Institute for Biophysical Chemistry, Hannover Medical School, Hannover, Germany.
  • Sarikidi A; Department of Diagnostic and Interventional Neuroradiology, Hannover Medical School, Hannover, Germany.
  • Auber B; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Raab P; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Christians A; Department of Human Genetics, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
  • Preller M; Department of Diagnostic and Interventional Neuroradiology, Hannover Medical School, Hannover, Germany.
  • Petri S; Department of Human Genetics, Hannover Medical School, Carl-Neuberg-Straße 1, 30625, Hannover, Germany.
  • Weber RG; Institute for Biophysical Chemistry, Hannover Medical School, Hannover, Germany.
J Neurol ; 267(9): 2732-2743, 2020 Sep.
Article em En | MEDLINE | ID: mdl-32447552
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha