A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Samankaltaisia teoksia

• The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.
  Tekijä: Meggouh, F, et al.
  Julkaistu: (1998)
• 4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects
  Tekijä: Iourov, Ivan Y., et al.
  Julkaistu: (2018)
• Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma
  Tekijä: Azzedine, H., et al.
  Julkaistu: (2003)
• SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease.
  Tekijä: Hanash, A, et al.
  Julkaistu: (1997)
• Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.
  Tekijä: Lopes, J., et al.
  Julkaistu: (1996)