Identification and molecular characterization of a novel 3′ mutation in RUNX1 in a family with familial platelet disorder

Leuk Lymphoma. 2010 Oct;51(10):1931-5. doi: 10.3109/10428194.2010.503821.
No abstract available

Publication types

  • Letter

MeSH terms

  • Acute Disease
  • Base Sequence
  • Blood Platelet Disorders / genetics*
  • Codon, Nonsense
  • Core Binding Factor Alpha 2 Subunit / genetics*
  • DNA Mutational Analysis
  • Exons / genetics
  • Family Health
  • Female
  • Germ-Line Mutation
  • Humans
  • Leukemia, Myeloid / genetics
  • Male
  • Mutation*
  • Pedigree

Substances

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