Mutations in the Norrie disease gene: a new mutation in a Japanese family

Br J Ophthalmol. 1995 Jul;79(7):703-4. doi: 10.1136/bjo.79.7.703.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Blindness / genetics*
  • Genetic Linkage
  • Humans
  • Male
  • Pedigree
  • Point Mutation*
  • X Chromosome