Acute myeloid leukemia in a child with familial platelet disorder and a cryptic runx1 intragenic deletion

Pediatr Hematol Oncol. 2022 Sep;39(6):580-585. doi: 10.1080/08880018.2022.2035028. Epub 2022 Feb 9.
No abstract available

Publication types

  • Letter

MeSH terms

  • Blood Platelet Disorders* / genetics
  • Child
  • Core Binding Factor Alpha 2 Subunit / genetics
  • Humans
  • Leukemia, Myeloid, Acute* / genetics
  • Mutation

Substances

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