Co-occurrence of type I CALR and two MPL mutations in patient with primary myelofibrosis

Ann Hematol. 2017 Aug;96(8):1417-1418. doi: 10.1007/s00277-017-3022-x. Epub 2017 May 13.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Alleles
  • Biopsy
  • Bone Marrow / pathology
  • Calreticulin / genetics*
  • DNA Mutational Analysis / methods*
  • Diagnostic Errors
  • Disease Progression
  • False Negative Reactions
  • Female
  • Frameshift Mutation
  • Humans
  • Limit of Detection
  • Middle Aged
  • Mutation, Missense*
  • Primary Myelofibrosis / diagnosis
  • Primary Myelofibrosis / genetics*
  • Receptors, Thrombopoietin / genetics*
  • Sequence Analysis, DNA
  • Thrombocythemia, Essential / diagnosis

Substances

  • CALR protein, human
  • Calreticulin
  • Receptors, Thrombopoietin
  • MPL protein, human