Color Vision Defects

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  Subject Areas on Research

  • Characterization of Ebola Virus-Associated Eye Disease. 
  • Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies. 
  • Identification of variants in CNGA3 as cause for achromatopsia by exome sequencing of a single patient. 
  • Macular photostress and visual experience between microscope and intracameral illumination during cataract surgery. 
  • Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy. 
  • Pigmented paravenous retinochoroidal atrophy. Discordant expression in monozygotic twins. 
  • Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. 
  • Visual pigments, blue cone monochromasy, and retinitis pigmentosa. 
  • X-linked high myopia associated with cone dysfunction.