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Functionally relevant RNA helicase mutations in familial and sporadic myeloid malignancies
Iléana Antony-Debré1, Ulrich Steidl1
1Department of Cell Biology and Department of Medicine (Oncology), Albert Einstein College of Medicine/Montefiore Medical Center, New York, NY 10461, USA.
Cancer Cell
|May 13, 2015
Abstract:
In this issue of Cancer Cell, Polprasert and colleagues identified recurrent mutations in the DEAD/H-box RNA helicase gene DDX41 in familial and acquired cases of myelodsyplasia and acute myeloid leukemia. These mutations induce defects in RNA splicing and represent a new class of mutations in myeloid malignancies.
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