FIP1L1/RARA with breakpoint at FIP1L1 intron 13: a variant translocation in acute promyelocytic leukemia

Haematologica. 2011 Oct;96(10):1565-6. doi: 10.3324/haematol.2011.047134. Epub 2011 Jul 12.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Base Sequence
  • Chromosome Breakpoints*
  • Chromosomes, Human, Pair 17
  • Female
  • Humans
  • Introns*
  • Karyotype
  • Leukemia, Promyelocytic, Acute / genetics*
  • Leukemia, Promyelocytic, Acute / pathology
  • Molecular Sequence Data
  • Receptors, Retinoic Acid / genetics*
  • Retinoic Acid Receptor alpha
  • Translocation, Genetic*
  • mRNA Cleavage and Polyadenylation Factors / genetics*

Substances

  • FIP1L1 protein, human
  • RARA protein, human
  • Receptors, Retinoic Acid
  • Retinoic Acid Receptor alpha
  • mRNA Cleavage and Polyadenylation Factors