VSX1 mutation and corneal dystrophies

Ophthalmology. 2005 Jan;112(1):170-1; author reply 171-2. doi: 10.1016/j.ophtha.2004.10.017.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple*
  • Auditory Perceptual Disorders / diagnosis
  • Auditory Perceptual Disorders / genetics
  • Corneal Dystrophies, Hereditary / diagnosis
  • Corneal Dystrophies, Hereditary / genetics*
  • Craniofacial Abnormalities / genetics
  • Empty Sella Syndrome / genetics
  • Endothelium, Corneal / abnormalities*
  • Eye Abnormalities / diagnosis
  • Eye Abnormalities / genetics*
  • Eye Proteins / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Keratoconus / diagnosis
  • Keratoconus / genetics*
  • Mutation*
  • Retinal Diseases / diagnosis
  • Retinal Diseases / genetics

Substances

  • Eye Proteins
  • Homeodomain Proteins
  • VSX1 protein, human