Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNA

J Neurol. 1995 Mar;242(4):253-5. doi: 10.1007/BF00919602.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • DNA, Mitochondrial / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mitochondrial Myopathies / complications*
  • Point Mutation*
  • Recurrence
  • Respiratory Insufficiency / etiology*

Substances

  • DNA, Mitochondrial