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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). [electronic resource] by
- Misu, K
- Yoshihara, T
- Shikama, Y
- Awaki, E
- Yamamoto, M
- Hattori, N
- Hirayama, M
- Takegami, T
- Nakashima, K
- Sobue, G
Producer: 20001222
In:
Journal of neurology, neurosurgery, and psychiatry vol. 69
Availability: No items available.
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