A novel null mutation in the rhodopsin gene causing late onset autosomal dominant retinitis pigmentosa

Hum Mutat. 1996;7(2):180. doi: 10.1002/humu.1380070202.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Codon
  • Genes, Dominant
  • Humans
  • Molecular Sequence Data
  • Point Mutation*
  • Polymorphism, Single-Stranded Conformational
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*

Substances

  • Codon
  • Rhodopsin