EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome

J Neurol. 2016 Jul;263(7):1456-8. doi: 10.1007/s00415-016-8153-9. Epub 2016 May 9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • DNA Mutational Analysis
  • Early Growth Response Protein 2 / genetics*
  • Female
  • Hereditary Sensory and Motor Neuropathy / genetics*
  • Hereditary Sensory and Motor Neuropathy / pathology
  • Hereditary Sensory and Motor Neuropathy / physiopathology*
  • Humans
  • Mutation / genetics*

Substances

  • EGR2 protein, human
  • Early Growth Response Protein 2