Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family

Acta Ophthalmol. 2011 Mar;89(2):e213-5. doi: 10.1111/j.1755-3768.2009.01802.x.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Czech Republic
  • Eye Proteins / genetics*
  • Female
  • Gene Amplification
  • Genetic Diseases, X-Linked / genetics*
  • Genotype
  • Humans
  • Male
  • Microsatellite Repeats
  • Molecular Biology
  • Mutation / genetics*
  • Pedigree
  • Polymerase Chain Reaction
  • Retinitis Pigmentosa / genetics*
  • White People

Substances

  • Eye Proteins
  • RPGR protein, human