NPM1 mutation in AML: WHO and why?

Research output: Contribution to journalEditorialpeer-review

4 Citations (Scopus)

Abstract

In this issue, Pasqualucci and colleagues show that the nucleophosmin (NPM1) mutation can be found in multiple myeloid lineages in AML, carrying implications for its cellular origins. They also suggest the recognition of this subset of AML in the World Health Organization (WHO) classification of mycloid neoplasms
Original languageEnglish
Pages (from-to)3965 - 3965
Number of pages1
JournalBlood
Volume108
Issue number13
Publication statusPublished - 15 Dec 2006

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