Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1

Clin Genet. 2006 Sep;70(3):253-6. doi: 10.1111/j.1399-0004.2006.00669.x.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Charcot-Marie-Tooth Disease / genetics*
  • Child
  • Connexins / genetics
  • DNA Mutational Analysis
  • Early Growth Response Protein 2 / genetics
  • Gap Junction beta-1 Protein
  • Humans
  • Korea
  • Male
  • Mutation*
  • Myelin P0 Protein / genetics
  • Myelin Proteins / genetics
  • Nuclear Proteins / genetics
  • Transcription Factors / genetics

Substances

  • Connexins
  • EGR2 protein, human
  • Early Growth Response Protein 2
  • LITAF protein, human
  • Myelin P0 Protein
  • Myelin Proteins
  • Nuclear Proteins
  • PMP22 protein, human
  • Transcription Factors