JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia

Leukemia. 2007 Feb;21(2):367-9. doi: 10.1038/sj.leu.2404484. Epub 2006 Dec 7.
No abstract available

Publication types

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

MeSH terms

  • Amino Acid Substitution*
  • Child
  • Child, Preschool
  • Chromosome Aberrations
  • Female
  • Humans
  • Infant
  • Janus Kinase 2 / genetics*
  • Karyotyping
  • Leukemia, Myelomonocytic, Acute / genetics*
  • Leukemia, Myelomonocytic, Chronic / genetics*
  • Male
  • Mutation*

Substances

  • JAK2 protein, human
  • Janus Kinase 2