ASXL1
B. L. Stein, D. M. Williams, Ch. O’Keefe, O. Rogers, R. G. Ingersoll, J. L. Spivak
Disruption of the ASXL1% gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
Haematologica 2011; 96(10): 1462-1469