JAK2V617F mutation can occur exclusively in the erythroid lineage and be absent in granulocytes and progenitor cells in classic myeloproliferative disorders

Am J Hematol. 2006 Oct;81(10):806-7. doi: 10.1002/ajh.20663.
No abstract available

Publication types

  • Letter

MeSH terms

  • Cell Lineage / genetics*
  • DNA Mutational Analysis / methods
  • Erythroid Cells
  • Flow Cytometry
  • Granulocytes
  • Humans
  • Janus Kinase 2 / genetics*
  • Myeloproliferative Disorders / genetics*
  • Point Mutation*
  • Stem Cells

Substances

  • JAK2 protein, human
  • Janus Kinase 2