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.
Saved in:
| Title: | 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. |
|---|---|
| Authors: | Meggendorfer, M1, Bacher, U1, Alpermann, T1, Haferlach, C1, Kern, W1, Gambacorti-Passerini, C2, Haferlach, T1, Schnittger, S1 |
| Source: | Leukemia (08876924). Sep2013, Vol. 27 Issue 9, p1852-1860. 9p. 2 Diagrams, 3 Charts, 1 Graph. |
| Database: | Academic Search Ultimate |
Be the first to leave a comment!
