[Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease]

Duodecim. 1994;110(7):681-6.
[Article in Finnish]
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Blindness / diagnosis
  • Blindness / epidemiology
  • Blindness / genetics*
  • Finland / epidemiology
  • Gyrate Atrophy / diagnosis
  • Gyrate Atrophy / epidemiology
  • Gyrate Atrophy / genetics*
  • Humans
  • Metabolism, Inborn Errors / diagnosis
  • Metabolism, Inborn Errors / epidemiology
  • Metabolism, Inborn Errors / genetics*
  • Metabolism, Inborn Errors / metabolism
  • Mutation
  • Ornithine / blood
  • Ornithine / metabolism*
  • Ornithine-Oxo-Acid Transaminase / deficiency*
  • Ornithine-Oxo-Acid Transaminase / metabolism

Substances

  • Ornithine
  • Ornithine-Oxo-Acid Transaminase