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April 01, 1997; 48 (Suppl 5) Articles

Congenital myasthenic syndromes caused by mutations in acetylcholine receptor genes

Andrew G. Engel, Kinji Ohno, Margherita Milone, Steven M. Sine
First published April 1, 1997, DOI: https://doi.org/10.1212/WNL.48.Suppl_5.28S
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Article Information

vol. 48 no. Suppl 5 28S-35S
DOI: 
https://doi.org/10.1212/WNL.48.Suppl_5.28S
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 April 1, 1997.
Copyright & Usage: 
Copyright 1997 by Advanstar Communications Inc.

Author Disclosures

    1. Andrew G. Engel, MD,
    2. Kinji Ohno, MD, PhD,
    3. Margherita Milone, MD, PhD and
    4. Steven M. Sine, PhD
  1. Andrew G. Engel, MD,
  2. Kinji Ohno, MD, PhD,
  3. Margherita Milone, MD, PhD and
  4. Steven M. Sine, PhD
  1. From the Department of Neurology and Muscle Research Laboratory (Drs. Engel, Ohno, Milone), and Department of Physiology and Receptor Biology Laboratory (Dr. Sine), Mayo Clinic, Rochester, MN.
  2. Supported by NIH grants NS6277 (to AGE) and NS31744 (to SMS), by a Muscular Dystrophy Association research grant (to AGE), by a Muscular Dystrophy Association research fellowship (to KO), and by an Italian Telethon award (to MM).
  3. Address correspondence and reprint requests to Dr. Andrew G. Engel, Department of Neurology and Muscle Research Laboratory, Mayo Clinic, 200 First Street SW, Rochester, MN 55905.
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