Cryptic insertion of KMT2A, a rare t(9;11) variant

Blood. 2021 Apr 1;137(13):1843. doi: 10.1182/blood.2020010442.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 9
  • Histone-Lysine N-Methyltransferase / genetics*
  • Humans
  • INDEL Mutation
  • Male
  • Myeloid-Lymphoid Leukemia Protein / genetics*
  • Pancytopenia / genetics*
  • Translocation, Genetic

Substances

  • KMT2A protein, human
  • Myeloid-Lymphoid Leukemia Protein
  • Histone-Lysine N-Methyltransferase