Molecular basis of ornithine aminotransferase defect in gyrate atrophy

Prog Clin Biol Res. 1991:362:191-219.
No abstract available

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • DNA / analysis
  • Gyrate Atrophy / enzymology*
  • Gyrate Atrophy / genetics
  • Humans
  • Molecular Sequence Data
  • Ornithine-Oxo-Acid Transaminase / deficiency
  • Ornithine-Oxo-Acid Transaminase / genetics*
  • Polymorphism, Restriction Fragment Length
  • RNA, Messenger / genetics

Substances

  • RNA, Messenger
  • DNA
  • Ornithine-Oxo-Acid Transaminase