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Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.
Tilch, Erik; Schormair, Barbara; Zhao, Chen; Salminen, Aaro V; Antic Nikolic, Ana; Holzknecht, Evi; Högl, Birgit; Poewe, Werner; Bachmann, Cornelius G; Paulus, Walter; Trenkwalder, Claudia; Oertel, Wolfgang H; Hornyak, Magdolna; Fietze, Ingo; Berger, Klaus; Lichtner, Peter; Gieger, Christian; Peters, Annette; Müller-Myhsok, Bertram; Hoischen, Alexander; Winkelmann, Juliane; Oexle, Konrad.
Afiliação
  • Tilch E; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Schormair B; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Zhao C; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Salminen AV; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Antic Nikolic A; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Holzknecht E; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Högl B; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Poewe W; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Bachmann CG; Department of Neurology, Paracelsus Clinic, Osnabrück, Germany.
  • Paulus W; Department of Clinical Neurophysiology, University Medical Center, Georg August University Göttingen, Göttingen, Germany.
  • Trenkwalder C; Clinic for Neurosurgery, University Medical Center, Georg August University Göttingen, Göttingen, Germany.
  • Oertel WH; Center of Parkinsonism and Movement Disorders, Paracelsus-Elena Hospital, Kassel, Germany.
  • Hornyak M; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Neurogenomics, Neuherberg, Germany.
  • Fietze I; Neuropsychiatry Center Erding/Munich, Erding, Germany.
  • Berger K; Department of Cardiology and Angiology, Center of Sleep Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Lichtner P; Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany.
  • Gieger C; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Human Genetics, Neuherberg, Germany.
  • Peters A; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Epidemiology II, Neuherberg, Germany.
  • Müller-Myhsok B; Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Institute of Epidemiology II, Neuherberg, Germany.
  • Hoischen A; Munich Cluster for Systems Neurology, Munich, Germany.
  • Winkelmann J; Max Planck Institute of Psychiatry, Munich, Germany.
  • Oexle K; Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Ann Neurol ; 87(2): 184-193, 2020 02.
Article em En | MEDLINE | ID: mdl-31788832
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome das Pernas Inquietas / Análise Mutacional de DNA / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Ann 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 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome das Pernas Inquietas / Análise Mutacional de DNA / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Ann Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha