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January 01, 1996; 46 (1) Article

Association of the mitochondrial 8344 MERRF mutation with maternally inherited spinocerebellar degeneration and Leigh disease

N. Howell, I. Kubacka, R. Smith, F. Frerman, J. K. Parks, W. D. Parker
First published January 1, 1996, DOI: https://doi.org/10.1212/WNL.46.1.219
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Article Information

vol. 46 no. 1 219-222
DOI: 
https://doi.org/10.1212/WNL.46.1.219
PubMed: 
8559379
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 January 1, 1996.
Copyright & Usage: 
Copyright 1996 by Advanstar Communications Inc.

Author Disclosures

    1. N. Howell, PhD,
    2. I. Kubacka, MS,
    3. R. Smith, MD, PhD,
    4. F. Frerman, PhD,
    5. J. K. Parks, BA and
    6. W. D. Parker Jr, MD
  1. N. Howell, PhD,
  2. I. Kubacka, MS,
  3. R. Smith, MD, PhD,
  4. F. Frerman, PhD,
  5. J. K. Parks, BA and
  6. W. D. Parker Jr, MD
  1. From the Departments of Radiation Therapy and Human Biological Chemistry and Genetics (Dr. Howell and I. Kubacka), The University of Texas Medical Branch, Galveston, TX; the Departments of Neurology (Dr. Smith) and Pediatrics (Drs. Smith and Frerman), The University of Colorado School of Medicine, Denver, CO; the Departments of Neurology and Pediatrics (J. Parks and Dr. Parker), The University of Virginia School of Medicine, Charlottesville, VA.
  2. Supported by NIH grants NS25382 (W.D.P.) and GM33683 (N.H.), and by NIH grant RR-69 from the General Clinical Research Centers Program (W.D.P.).
  3. Received February 22, 1995. Accepted in final form May 1, 1995.
  4. Address correspondence and reprint requests to Dr. Neil Howell, Biology Division F56, Department of Radiation Therapy, The University of Texas Medical Branch, Galveston, TX 77555-0656.
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