A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus

Hum Mutat. 1996;7(4):358-60. doi: 10.1002/(SICI)1098-1004(1996)7:4<358::AID-HUMU11>3.0.CO;2-1.
No abstract available

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cardiomyopathies / complications
  • Cardiomyopathies / genetics*
  • DNA, Mitochondrial
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / genetics*
  • Humans
  • MELAS Syndrome / complications
  • MELAS Syndrome / genetics*
  • Molecular Sequence Data
  • Mutation
  • NADH Dehydrogenase / genetics*
  • RNA / genetics
  • RNA, Mitochondrial
  • RNA, Transfer, Leu / genetics*
  • Syndrome

Substances

  • DNA, Mitochondrial
  • RNA, Mitochondrial
  • RNA, Transfer, Leu
  • RNA
  • NADH Dehydrogenase