Adding WT1 to childhood AML alphabet soup

Research output: Contribution to journalComment/debatepeer-review


In this issue of Blood, Hollink and colleagues establish WT1 mutations as a worthy addition to a growing list of molecular abnormalities that promise to improve the biologic understanding and treatment of intermediate-risk AML.

Original languageEnglish (US)
Pages (from-to)5696-5697
Number of pages2
Issue number23
StatePublished - 2009

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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