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An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)
- Dr Gen Sobuesobueg{at}med.nagoya-u.ac.jp
Citation
An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)
Publication history
- Received April 7, 2000
- Revised July 5, 2000
- Accepted July 19, 2000
- First published December 1, 2000.
Online issue publication
December 01, 2000
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Journal of Neurology, Neurosurgery, and Psychiatry