A new PTPN11 mutation in juvenile myelomonocytic leukaemia associated with Noonan syndrome

Acta Paediatr. 2005 May;94(5):636-7. doi: 10.1111/j.1651-2227.2005.tb01955.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Infant
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Leukemia, Myelomonocytic, Acute / complications*
  • Male
  • Noonan Syndrome / complications*
  • Noonan Syndrome / genetics*
  • 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