Rare Causes of Acute Coronary Syndrome: The JAK2 V617F Mutation-Positive Myeloproliferative Neoplasms: A Cardio-Hematological Perspective

Thromb Haemost. 2022 Aug;122(8):1429-1431. doi: 10.1055/a-1742-0361. Epub 2022 Jan 17.
No abstract available

Publication types

  • Letter

MeSH terms

  • Acute Coronary Syndrome* / genetics
  • Humans
  • Janus Kinase 2 / genetics
  • Mutation
  • Myeloproliferative Disorders* / complications
  • Myeloproliferative Disorders* / diagnosis
  • Myeloproliferative Disorders* / genetics
  • Neoplasms*

Substances

  • JAK2 protein, human
  • Janus Kinase 2