(Q3281259)

English

Charcot-Marie-Tooth disease type 4

Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has material basis in autosomal recessive inheritance

  • hereditary motor and sensory neuropathy Russe type
  • distal hereditary motor neuropathy
  • spinal CMT
  • hereditary motor and sensory neuropathy
  • AR-CMT1
  • Autosomal recessive demyelinating Charcot-Marie-Tooth
  • CMT4

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