Homozygous mutation (L527R) of TGFBI in an individual with lattice corneal dystrophy

Br J Ophthalmol. 2005 Jun;89(6):771-3. doi: 10.1136/bjo.2004.056168.
No abstract available

Publication types

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

MeSH terms

  • Amyloidosis / genetics
  • Corneal Dystrophies, Hereditary / genetics*
  • DNA Mutational Analysis
  • Homozygote
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Proteins / genetics*

Substances

  • Proteins