FIG4 mutations leading to parkinsonism and a phenotypical continuum between CMT4J and Yunis Varón syndrome.

Zimmermann M1, Schuster S2, Boesch S3, Korenke GC4, Mohr J5, Reichbauer J6, Kernstock C7, Kotzot D8, Spahlinger V6, Schüle-Freyer R2, Schöls L2.
  1. Department of Neurology and Hertie Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany; German Center for Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany. Electronic address: milan.zimmermann@med.uni-tuebingen.de..
  2. Department of Neurology and Hertie Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany; German Center for Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
  3. Department of Neurology, Medical University, Christoph-Probst-Platz 52, 6020, Innsbruck, Austria.
  4. Department of Neuropediatrics, University of Oldenburg, Rahel-Straus-Straße 10, 26133, Oldenburg, Germany.
  5. Center for Genomics and Transcriptomics (CeGaT) GmbH and Practice for Human Genetics, Paul-Ehrlich-Straße 23, 72076, Tübingen, Germany.
  6. Department of Neurology and Hertie Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
  7. University Eye Hospital, Center for Ophthalmology, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Germany.
  8. Institute of Human Genetics, Medical University Innsbruck, Christoph-Probst-Platz 52, 6020, Innsbruck, Austria; Division of Clinical Genetics, Department of Pediatrics, Paracelsus Medical University, Strubergasse 21, 5020, Salzburg, Austria.