Article
Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations.
Haematologica - 1 Jul 2015
Al Assaf Carla, Van Obbergh Florence, Billiet Johan, Lierman Els, Devos Timothy, Graux Carlos, Hervent Anne-Sophie, Emmerechts Jan, Tousseyn Thomas, De Paepe Pascale, Papadopoulos Petros, Michaux Lucienne, Vandenberghe Peter
Abstract excerpt
The JAK2 V617F mutation, the thrombopoietin receptor MPL W515K/L mutation and calreticulin (CALR) mutations are mutually exclusive in essential thrombocythemia and support a novel molecular categorization of essential thrombocythemia. CALR mutations account for approximately 30% of cases of essential thrombocythemia. In a retrospective study, we examined the frequency of MPL and CALR mutations in JAK2...
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