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Pearls & Oy-sters: Family history of Huntington disease disguised a case of dentatorubral-pallidoluysian atrophy.
Tunc, Sinem; Tadic, Vera; Zühlke, Christine; Hellenbroich, Yorck; Brüggemann, Norbert.
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  • Tunc S; From the Institute of Neurogenetics (S.T., V.T., N.B.), Department of Neurology (S.T., V.T., N.B.), and Institute of Human Genetics (C.Z., Y.H.), University of Lübeck, Germany.
  • Tadic V; From the Institute of Neurogenetics (S.T., V.T., N.B.), Department of Neurology (S.T., V.T., N.B.), and Institute of Human Genetics (C.Z., Y.H.), University of Lübeck, Germany.
  • Zühlke C; From the Institute of Neurogenetics (S.T., V.T., N.B.), Department of Neurology (S.T., V.T., N.B.), and Institute of Human Genetics (C.Z., Y.H.), University of Lübeck, Germany.
  • Hellenbroich Y; From the Institute of Neurogenetics (S.T., V.T., N.B.), Department of Neurology (S.T., V.T., N.B.), and Institute of Human Genetics (C.Z., Y.H.), University of Lübeck, Germany.
  • Brüggemann N; From the Institute of Neurogenetics (S.T., V.T., N.B.), Department of Neurology (S.T., V.T., N.B.), and Institute of Human Genetics (C.Z., Y.H.), University of Lübeck, Germany. norbert.brueggemann@neuro.uni-luebeck.de.
Neurology ; 90(3): 142-143, 2018 01 16.
Article en En | MEDLINE | ID: mdl-29335306
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Epilepsias Mioclónicas Progresivas Tipo de estudio: Diagnostic_studies Idioma: En Revista: Neurology Año: 2018 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Epilepsias Mioclónicas Progresivas Tipo de estudio: Diagnostic_studies Idioma: En Revista: Neurology Año: 2018 Tipo del documento: Article