Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21). Article uri icon

Overview

publication date

  • May 15, 2015

Research

keywords

  • Chromosomes, Human, Pair 21
  • Chromosomes, Human, Pair 8
  • Leukemia, Myeloid, Acute
  • Mutation
  • Repressor Proteins
  • Transcription Factors
  • Translocation, Genetic

Identity

Scopus Document Identifier

  • 84954203227

Digital Object Identifier (DOI)

  • 10.3109/10428194.2015.1037754

PubMed ID

  • 25856206

Additional Document Info

volume

  • 57

issue

  • 1