| Literature DB >> 17768124 |
Michela Palmisano, Tiziana Grafone, Emanuela Ottaviani, Nicoletta Testoni, Michele Baccarani, Giovanni Martinelli.
Abstract
NPM1 mutations have been reported to be the most frequent mutations in acute myeloid leukemia (AML). They are associated with a wide spectrum of morphologic subtypes of AML, normal karyotype and FLT3 mutations. The high frequency of NPM1 mutations might provide a suitable marker for monitoring residual disease of AML.Entities:
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Year: 2007 PMID: 17768124 DOI: 10.3324/haematol.11202
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941