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November 01, 1993; 43 (11) Article

Genetics of facioscapulohumeral muscular dystrophy

New mutations in sporadic cases

R. C. Griggs, R. Tawil, D. Storvick, J. R. Mendell, M. R. Altherr
First published November 1, 1993, DOI: https://doi.org/10.1212/WNL.43.11.2369
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Article Information

vol. 43 no. 11 2369
DOI: 
https://doi.org/10.1212/WNL.43.11.2369
PubMed: 
8232958
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. R. C. Griggs, MD,
    2. R. Tawil, MD,
    3. D. Storvick, MS,
    4. J. R. Mendell, MD and
    5. M. R. Altherr, PhD
  1. R. C. Griggs, MD,
  2. R. Tawil, MD,
  3. D. Storvick, MS,
  4. J. R. Mendell, MD and
  5. M. R. Altherr, PhD
  1. Department of Neurology, School of Medicine and Dentistry (Drs. Griggs and Tawil, and D. Storvick), University of Rochester, Rochester, NY; the Department of Neurology (Dr. Mendell), Ohio State University, Columbus, OH; and the Center for Human Genome Studies (Dr. Altherr), LANL, Los Alamos, NM.

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