Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.

Lignende værker

• Gyrate atrophy of the choroid and retina: ERG of the neural retina and the pigment epithelium.
  af: Raitta, C, et al.
  Udgivet: (1990)
• Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
  af: Valle, D, et al.
  Udgivet: (1977)
• Gyrate atrophy of the choroid and retina with hyperornithinemia: characterization of mutant liver L-ornithine:2-oxoacid aminotransferase kinetics.
  af: Sipilä, I, et al.
  Udgivet: (1981)
• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  af: Mitchell, G A, et al.
  Udgivet: (1988)
• The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.
  af: Ramesh, V, et al.
  Udgivet: (1988)