Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Am J Hum Genet. 1992 Mar;50(3):655-7.
No abstract available

Publication types

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

MeSH terms

  • Acidosis, Lactic / genetics
  • Base Sequence
  • Cerebrovascular Disorders / genetics
  • DNA, Mitochondrial / genetics*
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Mothers
  • Mutation
  • Neuromuscular Diseases / genetics*
  • Oligonucleotide Probes
  • Pedigree
  • Syndrome

Substances

  • DNA, Mitochondrial
  • Oligonucleotide Probes