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Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe

Authors

  • J Schicks,

    1. Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
    2. German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany
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  • M Synofzik,

    1. Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
    2. German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany
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  • C Beetz,

    1. Institute of Clinical Chemistry, University of Jena, Jena, Germany
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  • F Schiele,

    1. Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
    2. German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany
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  • L Schöls

    Corresponding author
    1. Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
    2. German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen, Tübingen, Germany
      Dr Ludger Schöls
      Department of Neurology
      Hertie-Institute for Clinical Brain Research
      and German Centre of Neurodegenerative Diseases
      Hoppe-Seyler-Street 3
      University of Tübingen
      72076 Tübingen
      Germany
      Tel.: +49 7071 2980412
      Fax: +49 7071 295957
      e-mail: ludger.schoels@uni-tuebingen.de
    Search for more papers by this author

Dr Ludger Schöls
Department of Neurology
Hertie-Institute for Clinical Brain Research
and German Centre of Neurodegenerative Diseases
Hoppe-Seyler-Street 3
University of Tübingen
72076 Tübingen
Germany
Tel.: +49 7071 2980412
Fax: +49 7071 295957
e-mail: ludger.schoels@uni-tuebingen.de

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