Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.

Similar Items

• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  od: Mitchell, G A, i dr.
  Izdano: (1988)
• At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
  od: Mitchell, G A, i dr.
  Izdano: (1989)
• Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina.
  od: Shih, V E, i dr.
  Izdano: (1978)
• Gyrate atrophy of the choroid and retina: amino acid metabolism and correction of hyperornithinemia with an arginine-deficient diet.
  od: Valle, D, i dr.
  Izdano: (1980)
• Gyrate atrophy of the choroid and retina with hyperornithinemia: characterization of mutant liver L-ornithine:2-oxoacid aminotransferase kinetics.
  od: Sipilä, I, i dr.
  Izdano: (1981)