An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.

Lignende værker

• At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
  af: Mitchell, G A, et al.
  Udgivet: (1989)
• Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
  af: Valle, D, et al.
  Udgivet: (1977)
• Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina
  af: Wang, Tao, et al.
  Udgivet: (2000)
• Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina.
  af: Shih, V E, et al.
  Udgivet: (1978)
• Gyrate atrophy of the choroid and retina: characterization of mutant ornithine aminotransferase and mechanism of response to vitamin B6.
  af: Kennaway, N G, et al.
  Udgivet: (1989)