(Q27164483)

English

Charcot-Marie-Tooth disease axonal type 2L

Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene

  • CMT2L
  • Charcot-Marie-Tooth neuropathy axonal type 2L
  • autosomal dominant Charcot-Marie-Tooth disease type 2L
  • autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2L
  • CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L
  • Charcot-Marie-Tooth Neuropathy, Axonal, Type 2L
  • CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L
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