The clinical implication of SRSF2 mutation in patients with myelodysplastic syndrome and its stability during disease evolution
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Title
The clinical implication of SRSF2 mutation in patients with myelodysplastic syndrome and its stability during disease evolution
Authors
Keywords
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Journal
BLOOD
Volume 120, Issue 15, Pages 3106-3111
Publisher
American Society of Hematology
Online
2012-08-30
DOI
10.1182/blood-2012-02-412296
References
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Related references
Note: Only part of the references are listed.- Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes
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- Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
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- Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML
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