Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.

相似書籍

• Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.
  由: Hotta, Y, et al.
  出版: (1989)
• Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6.
  由: Kennaway, N G, et al.
  出版: (1989)
• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  由: Mitchell, G A, et al.
  出版: (1988)
• Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy.
  由: McClatchey, A I, et al.
  出版: (1990)
• The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.
  由: Ramesh, V, et al.
  出版: (1988)