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A unique clonal JAK2 mutation leading to constitutive signaling causes polycythaemica vera
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Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
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V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis
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Outcome of allogeneic stem cell transplantation in patients with myelofibrosis
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