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October 01, 1974; 24 (10) Article

Pyruvate oxidation in neuromuscular diseases

Evidence of a genetic defect in two families with the clinical syndrome of Friedreich's ataxia*

R. A. PIETER KARK, JOHN P. BLASS, W. KING ENGEL
First published October 1, 1974, DOI: https://doi.org/10.1212/WNL.24.10.964
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Article Information

vol. 24 no. 10 964
DOI: 
https://doi.org/10.1212/WNL.24.10.964
PubMed: 
4370305
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 October 1, 1974.
Copyright & Usage: 
© 1974 by the American Academy of Neurology

Author Disclosures

    1. R. A. PIETER KARK, M.D.,
    2. JOHN P. BLASS, M.D.,Ph.D. and
    3. W. KING ENGEL, M.D.
  1. R. A. PIETER KARK, M.D.,
  2. JOHN P. BLASS, M.D.,Ph.D. and
  3. W. KING ENGEL, M.D.
  1. Medical Neurology Branch, Natinal Institute of Neurological Diseases, National Institutes of Health, United States Public Health Service, Department of Health, Education, and Welfare, Bethesda, Maryland (Dr. Engel and Dr. Kark), and the Reed Neurological Research Center (Dr. Kark) and the Mental Retardation Program, Neuropsychiatric Institute (Dr. Blass and Dr. Kark). UCLA School of Medicine, Los Angeles, California.

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