Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype

Hum Mol Genet. 1995 Sep;4(9):1689-91. doi: 10.1093/hmg/4.9.1689.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Primers
  • Haplotypes
  • Humans
  • MELAS Syndrome / genetics*
  • Molecular Sequence Data
  • Phenotype
  • Point Mutation*
  • RNA / genetics*
  • RNA, Mitochondrial
  • RNA, Transfer, Leu / genetics*

Substances

  • DNA Primers
  • RNA, Mitochondrial
  • RNA, Transfer, Leu
  • RNA