JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia | Journal of Clinical Pathology

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JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia

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Cite this article as:: Pich A, Riera L, Beggiato E, et al

JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia

Journal of Clinical Pathology 2012;65:953-955.