ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category
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Open Access
- 22 December 2011
- journal article
- Published by American Society of Hematology in Blood
- Vol. 118 (26), 6920-6929
- https://doi.org/10.1182/blood-2011-08-368225
Abstract
The associations of mutations in the enhancer of trithorax and polycomb family gene ASXL1 with pretreatment patient characteristics, outcomes, and geKeywords
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