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November 01, 1993; 43 (11) Brief Communication

Progressive myoclonus epilepsy of Unverricht‐Lundborg type

A clinical and molecular genetic study of a family from the United States with four affected sibs

A.-E. Lehesjoki, R. Eldridge, J. Eldridge, B. J. Wilder, A. de la Chapelle
First published November 1, 1993, DOI: https://doi.org/10.1212/WNL.43.11.2384
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Article Information

vol. 43 no. 11 2384
DOI: 
https://doi.org/10.1212/WNL.43.11.2384
PubMed: 
8232963
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 November 1, 1993.
Copyright & Usage: 
© 1993 by the American Academy of Neurology

Author Disclosures

    1. A.-E. Lehesjoki, MD,
    2. R. Eldridge, MD,
    3. J. Eldridge, BS,
    4. B. J. Wilder, MD and
    5. A. de la Chapelle, MD
  1. A.-E. Lehesjoki, MD,
  2. R. Eldridge, MD,
  3. J. Eldridge, BS,
  4. B. J. Wilder, MD and
  5. A. de la Chapelle, MD
  1. Department of Medical Genetics, University of Helsinki, and the Folkhälsan Institute of Genetics (Drs. Lehesjoki and de la Chapelle), Helsinki, Finland; the Clinical Genetics Section (Dr. R. Eldridge), Clinical Epidemiology Branch, National Cancer Institute, and the Laboratory of Biochemistry (J. Eldridge), National Cancer Institute, National Institutes of Health, Bethesda, MD; and the Veterans Administration Hospital Medical Center and University of Florida College of Medicine (Dr. Wilder), Gainesville, FL.

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