A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy

J Neuromuscul Dis. 2019;6(3):385-387. doi: 10.3233/JND-190400.
No abstract available

Keywords: CMT; MT-ATP6; Neuropathy; mitochondria; myelopathy.

Publication types

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

MeSH terms

  • Charcot-Marie-Tooth Disease / diagnosis
  • Charcot-Marie-Tooth Disease / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mitochondrial Proton-Translocating ATPases / genetics*
  • Mutation / genetics*

Substances

  • MT-ATP6 protein, human
  • Mitochondrial Proton-Translocating ATPases