Functionally relevant RNA helicase mutations in familial and sporadic myeloid malignancies
- PMID: 25965566
- DOI: 10.1016/j.ccell.2015.04.013
Functionally relevant RNA helicase mutations in familial and sporadic myeloid malignancies
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.
Copyright © 2015 Elsevier Inc. All rights reserved.
Comment on
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Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms.Cancer Cell. 2015 May 11;27(5):658-70. doi: 10.1016/j.ccell.2015.03.017. Epub 2015 Apr 23. Cancer Cell. 2015. PMID: 25920683 Free PMC article.
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