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Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe
Authors:Schicks J  Synofzik M  Beetz C  Schiele F  Schöls L
Affiliation: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;3. Institute of Clinical Chemistry, University of Jena, Jena, Germany
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