Ultrastructural mitochondrial modifications characteristic of mitofusin 2 mutations (CMT2A)

J Peripher Nerv Syst. 2009 Sep;14(3):206-7. doi: 10.1111/j.1529-8027.2009.00234.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / pathology*
  • Child
  • Female
  • GTP Phosphohydrolases
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Mitochondria / ultrastructure*
  • Mitochondrial Proteins / genetics*
  • Mutation

Substances

  • Membrane Proteins
  • Mitochondrial Proteins
  • GTP Phosphohydrolases
  • MFN2 protein, human