Gyrate atrophy of the choroid and retina with hyperornithinemia: characterization of mutant liver L-ornithine:2-oxoacid aminotransferase kinetics.

Samankaltaisia teoksia

• Gyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginine.
  Tekijä: Sipilä, I, et al.
  Julkaistu: (1980)
• Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
  Tekijä: Valle, D, et al.
  Julkaistu: (1977)
• At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
  Tekijä: Mitchell, G A, et al.
  Julkaistu: (1989)
• Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.
  Tekijä: O'Donnell, J J, et al.
  Julkaistu: (1988)
• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  Tekijä: Mitchell, G A, et al.
  Julkaistu: (1988)