A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals

Eur J Haematol. 2010 Dec;85(6):552-3. doi: 10.1111/j.1600-0609.2010.01513.x. Epub 2010 Oct 28.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Core Binding Factor Alpha 2 Subunit / genetics*
  • Female
  • Humans
  • Leukemia, Myeloid, Acute / genetics*
  • Leukemia, Myeloid, Acute / therapy
  • Male
  • Mutation*
  • Pedigree
  • Propensity Score
  • Sex Factors
  • Stem Cell Transplantation
  • Thrombocytopenia / genetics*
  • Thrombocytopenia / therapy
  • Transplantation, Homologous

Substances

  • Core Binding Factor Alpha 2 Subunit
  • RUNX1 protein, human