Mutations in PTPN11 are rare in adult myelodysplastic syndromes and acute myeloid leukemia

Am J Hematol. 2004 Aug;76(4):417. doi: 10.1002/ajh.20134.
No abstract available

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Acute Disease
  • Adult
  • Age Factors
  • Child
  • Chromosomes, Human, Pair 7
  • DNA Mutational Analysis
  • Exons / genetics
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Leukemia, Myeloid / genetics*
  • Monosomy
  • Myelodysplastic Syndromes / genetics*
  • Polymerase Chain Reaction
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Protein Tyrosine Phosphatases / genetics*

Substances

  • Intracellular Signaling Peptides and Proteins
  • PTPN11 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
  • Protein Tyrosine Phosphatases