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Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31

  • Torbjoern G. Nygaard
  • , Deborah Raymond
  • , Caiping Chen
  • , Ichizo Nishino
  • , Paul E. Greene
  • , Danna Jennings
  • , Gary A. Heiman
  • , Christine Klein
  • , Rachel J. Saunders-Pullman
  • , Patricia Kramer
  • , Laurie J. Ozelius
  • , Susan B. Bressman

Research output: Contribution to journalArticlepeer-review

Abstract

Essential myoclonus-dystonia is a neurological condition characterized by myoclonic and dystonic muscle contractions and the absence of other neurological signs or laboratory abnormalities; it is often responsive to alcohol. The disorder may be familial with apparent autosomal dominant inheritance. We report a large kindred with essential familial myoclonus- dystonia and map a locus for the disorder to a 28-cM region of chromosome 7q21-q31.

Original languageEnglish (US)
Pages (from-to)794-798
Number of pages5
JournalAnnals of Neurology
Volume46
Issue number5
DOIs
StatePublished - 1999

Funding

FundersFunder number
National Institute of Neurological Disorders and StrokeR01NS026656

    ASJC Scopus subject areas

    • Neurology
    • Clinical Neurology

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