Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

Am J Hum Genet. 1998 Jul;63(1):274-9. doi: 10.1086/301905.
No abstract available

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 6 / genetics*
  • Color Perception / physiology
  • Electrophysiology
  • England
  • Eye Diseases / genetics*
  • Female
  • Genes, Dominant / genetics
  • Genetic Linkage
  • Haplotypes / genetics
  • Humans
  • Lod Score
  • Male
  • Microsatellite Repeats / genetics
  • Pedigree
  • Photoreceptor Cells / pathology*
  • Proteoglycans / genetics
  • Retina / pathology

Substances

  • Proteoglycans