Risk Alleles Associated with Neovascularization in a Pachychoroid Phenotype

Ophthalmology. 2016 Dec;123(12):2628-2630. doi: 10.1016/j.ophtha.2016.06.060. Epub 2016 Aug 6.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Apolipoproteins / genetics
  • Case-Control Studies
  • Choroid Diseases / diagnosis
  • Choroid Diseases / genetics*
  • Choroidal Neovascularization / diagnosis
  • Choroidal Neovascularization / genetics*
  • Complement C2
  • Complement C3 / genetics
  • Complement Factor B / genetics
  • Complement Factor H / genetics
  • Complement System Proteins / genetics*
  • Eye Proteins / genetics*
  • Factor XIII / genetics
  • Female
  • Gene Frequency*
  • Humans
  • Male
  • Middle Aged
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Proteins / genetics
  • Risk Factors
  • Wet Macular Degeneration / diagnosis
  • Wet Macular Degeneration / genetics*

Substances

  • ARMS2 protein, human
  • Apolipoproteins
  • CFH protein, human
  • CFHR4 protein, human
  • Complement C2
  • Complement C3
  • Eye Proteins
  • Proteins
  • Complement Factor H
  • Complement System Proteins
  • Factor XIII
  • factor XIIIb
  • Complement Factor B