Author reply: "MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy"

J Neurol Sci. 2017 Nov 15:382:166-167. doi: 10.1016/j.jns.2017.09.046. Epub 2017 Sep 30.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • DNA, Mitochondrial*
  • Humans
  • Mitochondria
  • Mutation
  • Optic Atrophy, Hereditary, Leber*
  • Virulence

Substances

  • DNA, Mitochondrial