The JAK2 V617F mutation is not a cause of central retinal vein occlusion

Thromb Haemost. 2008 Sep;100(3):515-6.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Female
  • Humans
  • Janus Kinase 2 / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Point Mutation
  • Retinal Vein / pathology*
  • Retinal Vein Occlusion / genetics*
  • Risk Factors
  • Thrombosis

Substances

  • JAK2 protein, human
  • Janus Kinase 2