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  • Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

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Neurogenetics
Research paper
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

Authors

  • Masato Obayashi Department of Neurology and Neurological Sciences, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Giovanni Stevanin Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France AP-HP, Groupe Hospitalier Pitié-Salpêtriére, Departement of Genetics and Cytogenetics, Paris, France Ecole Pratique des Hautes Etudes, Groupe de Neurogénétique, Paris, France PubMed articlesGoogle scholar articles
  • Matthis Synofzik Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, Tübingen, Germany German Centre of Neurodegenerative Diseases, University of Tübingen, Tübingen, Germany PubMed articlesGoogle scholar articles
  • Marie-Lorraine Monin Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France PubMed articlesGoogle scholar articles
  • Charles Duyckaerts Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France Laboratoire de Neuropathologie R. Escourolle, Groupe Hospitalier Pitié-Salpêtrière, 47 Blvd de l'Hôpital, Paris, France PubMed articlesGoogle scholar articles
  • Nozomu Sato Department of Neurology and Neurological Sciences, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Nathalie Streichenberger Pathology and Biochemistry, Groupement Hospitalier Est, Hospices Civils de Lyon/Claude Bernard University, Lyon, France PubMed articlesGoogle scholar articles
  • Alain Vighetto Neurology Department, Hôpital Pierre Wertheimer, Lyon, France PubMed articlesGoogle scholar articles
  • Virginie Desestret Neurology D, Hospices Civils de Lyon, Hôpital Neurologique, Bron, France Lyon Neuroscience Research Center, INSERM U1028/CNRS UMR 5292, Lyon, France Université de Lyon—Université Claude Bernard Lyon 1, Lyon, France PubMed articlesGoogle scholar articles
  • Christelle Tesson Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France Ecole Pratique des Hautes Etudes, Groupe de Neurogénétique, Paris, France PubMed articlesGoogle scholar articles
  • H-Erich Wichmann Institute of Epidemiology I, Helmholtz Zentrum München—German Research Center for Environmental Health, Neuherberg, Germany Institute of Medical Informatics, Biometry and Epidemiology, Chair of Epidemiology, Ludwig-Maximilians-Universität, Munich, Germany PubMed articlesGoogle scholar articles
  • Thomas Illig Unit for Molecular Epidemiology, Helmholtz Zentrum München—German Research Center for Environmental Health, Neuherberg, Germany PubMed articlesGoogle scholar articles
  • Johanna Huttenlocher Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany PubMed articlesGoogle scholar articles
  • Yasushi Kita Neurology Service, Hyogo Brain and Heart Center at Himeji, Himeji, Hyogo, Japan PubMed articlesGoogle scholar articles
  • Yuishin Izumi Department of Clinical Neuroscience, The University of Tokushima Graduate School, Tokushima, Japan PubMed articlesGoogle scholar articles
  • Hidehiro Mizusawa Department of Neurology and Neurological Sciences, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Ludger Schöls Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, Tübingen, Germany German Centre of Neurodegenerative Diseases, University of Tübingen, Tübingen, Germany PubMed articlesGoogle scholar articles
  • Thomas Klopstock Department of Neurology, Friedrich-Baur-Institute, Ludwig-Maximilians-Universität München, Munich, Germany German Network for Mitochondrial Disorders (mitoNET) DZNE—German Center for Neurodegenerative Diseases, Munich, Germany German Center for Vertigo and Balance Disorders, Munich, Germany PubMed articlesGoogle scholar articles
  • Alexis Brice Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France AP-HP, Groupe Hospitalier Pitié-Salpêtriére, Departement of Genetics and Cytogenetics, Paris, France PubMed articlesGoogle scholar articles
  • Kinya Ishikawa Department of Neurology and Neurological Sciences, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Alexandra Dürr Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France AP-HP, Groupe Hospitalier Pitié-Salpêtriére, Departement of Genetics and Cytogenetics, Paris, France PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Alexis Brice, Institut du Cerveau et de la Moelle épinière, Groupe Hospitalier Pitié-Salpêtrière, Paris 75013, France; alexis.brice{at}upmc.fr
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Citation

Obayashi M, Stevanin G, Synofzik M, et al
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion
Journal of Neurology, Neurosurgery & Psychiatry 2015;86:986-995.

Publication history

  • Received August 13, 2014
  • Revised October 17, 2014
  • Accepted November 3, 2014
  • First published December 4, 2014.
Online issue publication 
April 13, 2016

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