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April 01, 1997; 48 (4) Article

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot‐Marie‐Tooth disease

M. Kessali, R. Zemmouri, A. Guilbot, T. Maisonobe, A. Brice, E. LeGuern, D. Grid
First published April 1, 1997, DOI: https://doi.org/10.1212/WNL.48.4.867
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Article Information

vol. 48 no. 4 867-873
DOI: 
https://doi.org/10.1212/WNL.48.4.867
PubMed: 
9109869
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 the American Academy of Neurology

Author Disclosures

    1. M. Kessali, MD,
    2. R. Zemmouri, MD,
    3. A. Guilbot, MS,
    4. T. Maisonobe, MD,
    5. A. Brice, MD,
    6. E. LeGuern, MD, PhD and
    7. D. Grid, MD
  1. M. Kessali, MD,
  2. R. Zemmouri, MD,
  3. A. Guilbot, MS,
  4. T. Maisonobe, MD,
  5. A. Brice, MD,
  6. E. LeGuern, MD, PhD and
  7. D. Grid, MD
  1. From the Service de Neurologie (Drs. Kessali, Zemmouri, and Grid), CHU Mustapha, Algiers, Algeria; and the Fédération de Neurologie (Drs. Brice and LeGuern), U289 de l'INSERM (A. Guilbot and Drs. Brice and LeGuern), and the Laboratoire de Neuropathologie R. Escourolle (Dr. Maisonobe), Hopital de la Salpětrière, Paris, France.

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