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July 11, 2006; 67 (1) Brief Communications

Autosomal dominant monosymptomatic myotonia permanens

Eskild Colding-Jørgensen, Morten Duno, John Vissing
First published July 10, 2006, DOI: https://doi.org/10.1212/01.wnl.0000223838.88872.da
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Article Information

vol. 67 no. 1 153-155
DOI: 
https://doi.org/10.1212/01.wnl.0000223838.88872.da
PubMed: 
16832098
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published July 10, 2006.
Copyright & Usage: 
© 2006

Author Disclosures

    1. Eskild Colding-Jørgensen, MD,
    2. Morten Duno, PhD and
    3. John Vissing, MD
  1. Eskild Colding-Jørgensen, MD,
  2. Morten Duno, PhD and
  3. John Vissing, MD
  1. From the Department of Clinical Neurophysiology (E.C.-J.), Glostrup Hospital, University of Copenhagen, Glostrup, Denmark; Departments of Clinical Genetics (M.D.) and Neurology (J.V.), Neuromuscular Research Unit (J.V.), and the Copenhagen Muscle Research Centre (J.V.), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
  1. Address correspondence and reprint requests to Dr. Eskild Colding-Jørgensen, Department of Clinical Neurophysiology 19, Glostrup Hospital, University of Copenhagen, Ndr. Ringvej, DK-2600 Glostrup, Denmark; e-mail: escj{at}glostruphosp.kbhamt.dk
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