Vitreous phenotype: genotype correlation in Stickler syndrome

Graefes Arch Clin Exp Ophthalmol. 2002 Jan;240(1):63-5; author reply 66. doi: 10.1007/s00417-001-0380-8.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Child
  • Collagen Diseases / genetics
  • Collagen Diseases / pathology
  • Collagen Type II / genetics*
  • Collagen Type XI / genetics*
  • Female
  • Genotype
  • Humans
  • Mutation
  • Phenotype
  • Syndrome
  • Vitreous Body / pathology*
  • Vitreous Detachment / genetics*
  • Vitreous Detachment / pathology*

Substances

  • COL2A1 protein, human
  • Collagen Type II
  • Collagen Type XI