Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy

Genomics. 1992 Oct;14(2):553-4. doi: 10.1016/s0888-7543(05)80271-x.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acids / genetics
  • Base Sequence
  • Gyrate Atrophy / enzymology
  • Gyrate Atrophy / genetics*
  • Humans
  • Molecular Sequence Data
  • Mutation*
  • Ornithine-Oxo-Acid Transaminase / genetics*
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Sequence Deletion

Substances

  • Amino Acids
  • RNA, Messenger
  • Ornithine-Oxo-Acid Transaminase