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De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient.
Klein, Christine; Baumann, Hauke; Olschewski, Luisa; Hanssen, Henrike; Münchau, Alexander; Ferbert, Andreas; Brüggemann, Norbert; Lohmann, Katja.
Afiliación
  • Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Baumann H; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Olschewski L; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Hanssen H; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany; Department of Neurology, University Hospital Schleswig-Holstein, Campus Lübeck, Germany.
  • Münchau A; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Ferbert A; Department of Neurology, Klinikum Kassel, Kassel, Germany.
  • Brüggemann N; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany; Department of Neurology, University Hospital Schleswig-Holstein, Campus Lübeck, Germany.
  • Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany. Electronic address: katja.lohmann@neuro.uni-luebeck.de.
Parkinsonism Relat Disord ; 64: 337-339, 2019 07.
Article en En | MEDLINE | ID: mdl-30935829
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: N-Metiltransferasa de Histona-Lisina / Trastornos Distónicos / Discalculia Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans País/Región como asunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: N-Metiltransferasa de Histona-Lisina / Trastornos Distónicos / Discalculia Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Adult / Female / Humans País/Región como asunto: Asia Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania