Charcot-Marie-Tooth disease axonal type 2K (Q27164475)

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Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the GDAP1 gene on chromosome 8q
  • ARCMT2K
  • Charcot-Marie-Tooth neuropathy axonal type 2K
  • autosomal recessive Charcot-Marie-Tooth disease with hoarseness
  • autosomal recessive axonal CMT4C4
  • autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K
  • autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
  • Charcot-Marie-Tooth disease type 2K
  • CMT2K
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English
Charcot-Marie-Tooth disease axonal type 2K
Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the GDAP1 gene on chromosome 8q
  • ARCMT2K
  • Charcot-Marie-Tooth neuropathy axonal type 2K
  • autosomal recessive Charcot-Marie-Tooth disease with hoarseness
  • autosomal recessive axonal CMT4C4
  • autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K
  • autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
  • Charcot-Marie-Tooth disease type 2K
  • CMT2K

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