The molecular biology of Norrie's disease

Eye (Lond). 1994:8 ( Pt 5):491-6. doi: 10.1038/eye.1994.124.

Abstract

The Norrie's disease gene has been accurately located on the short arm of the X chromosome. The methodology underlying this achievement and the structure of the three-exon gene is described in this review article. The clinical implications of these recent advances are discussed. Allelic variants of Norrie's disease and the phenomenon of females affected by X-linked disease are also discussed.

Publication types

  • Review

MeSH terms

  • Chromosome Deletion
  • Chromosome Mapping
  • Cloning, Molecular
  • Female
  • Genetic Linkage*
  • Heterozygote
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Retina / abnormalities*
  • Retinal Detachment / genetics
  • Sex Chromosome Aberrations
  • Syndrome
  • X Chromosome*