CALR mutations in patients with essential thrombocythemia diagnosed in childhood and adolescence
2014
To the editor:
After the recent discovery of various mutations of the CALR gene, <10% of adult patients with essential thrombocythemia (ET) or primary myelofibrosis carry no identified molecular markers.[1][1],[2][2] More rarely, ET may occur also in children and adolescents.[3][3] We evaluated, by
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