Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3.

@article{Nelis2004AutosomalDA,
  title={Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12-q13.3.},
  author={Eva Nelis and Jos{\'e} Berciano and Nathalie Verpoorten and Katrien Coen and Ines Dierick and Veerle Van Gerwen and Onofre Combarros and Peter de Jonghe and Vincent Timmerman},
  journal={Journal of medical genetics},
  year={2004},
  volume={41 3},
  pages={193-7}
}
C harcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of disorders that involve the peripheral nervous system. It is characterised by progressive distal neurogenic muscular atrophy and weakness that initially affects the peroneal muscles and later the hands. Charcot-Marie-Tooth disease type 1 (CMT1), also called hereditary motor and sensory neuropathy type I (HMSN I), is a dominantly inherited demyelinating neuropathy characterised by reduced nerve conduction… CONTINUE READING