JAK2V617F mutation in patients with arterial thrombosis in the absence of overt myeloproliferative disease

J Thromb Haemost. 2009 Apr;7(4):722-5. doi: 10.1111/j.1538-7836.2009.03303.x. Epub 2009 Jan 24.
No abstract available

Publication types

  • Letter
  • Meta-Analysis

MeSH terms

  • Arterial Occlusive Diseases / epidemiology
  • Arterial Occlusive Diseases / genetics
  • Humans
  • Mutation, Missense*
  • Myeloproliferative Disorders
  • Prevalence
  • Thrombosis / epidemiology
  • Thrombosis / genetics*