LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States

Am J Ophthalmol. 2007 Dec;144(6):974-975. doi: 10.1016/j.ajo.2007.09.034.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Amino Acid Oxidoreductases / genetics*
  • Exfoliation Syndrome / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Genotype
  • Glaucoma, Open-Angle / genetics
  • Humans
  • Iowa / epidemiology
  • Male
  • Mutation*
  • Polymorphism, Single Nucleotide

Substances

  • Amino Acid Oxidoreductases
  • LOXL1 protein, human