Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder

Leuk Lymphoma. 2020 Jan;61(1):181-184. doi: 10.1080/10428194.2019.1648801. Epub 2019 Aug 6.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Core Binding Factor Alpha 2 Subunit / genetics
  • Female
  • Genomics
  • Germ-Line Mutation
  • Humans
  • Leukemia, Myeloid, Acute* / diagnosis
  • Leukemia, Myeloid, Acute* / genetics
  • Male
  • Middle Aged
  • Mutation
  • Myelodysplastic Syndromes* / diagnosis
  • Myelodysplastic Syndromes* / genetics
  • Pedigree

Substances

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