Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.

Samankaltaisia teoksia

• Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6.
  Tekijä: Kennaway, N G, et al.
  Julkaistu: (1989)
• Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.
  Tekijä: Mashima, Y, et al.
  Julkaistu: (1992)
• Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
  Tekijä: Valle, D, et al.
  Julkaistu: (1977)
• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  Tekijä: Mitchell, G A, et al.
  Julkaistu: (1988)
• 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)