Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP

Adv Exp Med Biol. 2003:533:1-11. doi: 10.1007/978-1-4615-0067-4_1.
No abstract available

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Chromosome Mapping
  • Cloning, Molecular
  • Eye Proteins / genetics*
  • Eye Proteins / metabolism
  • Genes, Dominant*
  • Genetic Linkage
  • Genetic Testing
  • Humans
  • IMP Dehydrogenase / genetics*
  • Microtubule-Associated Proteins
  • Molecular Sequence Data
  • Mutation
  • Pedigree
  • Retinitis Pigmentosa / genetics*
  • Retinitis Pigmentosa / physiopathology

Substances

  • Eye Proteins
  • Microtubule-Associated Proteins
  • RP1 protein, human
  • IMP Dehydrogenase
  • IMPDH1 protein, human