Characterization of cases with the rare cytogenetic abnormality i(7)(p10) reveals an association with IDH2-mutated AML

Blood Adv. 2024 Aug 13;8(15):4125-4128. doi: 10.1182/bloodadvances.2024013225.
No abstract available

MeSH terms

  • Adult
  • Aged
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 7 / genetics
  • Female
  • Humans
  • Isocitrate Dehydrogenase* / genetics
  • Leukemia, Myeloid, Acute* / genetics
  • Male
  • Middle Aged
  • Mutation*

Substances

  • Isocitrate Dehydrogenase
  • IDH2 protein, human