An unusual, activating insertion/deletion MPL mutant in primary myelofibrosis

Leukemia. 2017 Aug;31(8):1838-1839. doi: 10.1038/leu.2017.153. Epub 2017 May 22.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Amino Acid Sequence
  • Base Sequence
  • Female
  • Humans
  • INDEL Mutation*
  • Primary Myelofibrosis / genetics*
  • Receptors, Thrombopoietin / genetics*

Substances

  • Receptors, Thrombopoietin
  • MPL protein, human