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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
✍ Scribed by Meggendorfer, M; Bacher, U; Alpermann, T; Haferlach, C; Kern, W; Gambacorti-Passerini, C; Haferlach, T; Schnittger, S
- Book ID
- 120405727
- Publisher
- Nature Publishing Group
- Year
- 2013
- Tongue
- English
- Weight
- 453 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0887-6924
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