SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations
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| Description | scientific article published on 30 April 2013 |
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author: Claudia Haferlach Susanne Schnittger Torsten Haferlach Carlo Gambacorti-Passerini |
| Publication date | April 30, 2013 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |