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MPL mutations and palpable splenomegaly are independent risk factors for fibrotic progression in essential thrombocythemia

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Bibliographic Details
Published in:	Blood cancer journal (New York) 2016-10, Vol.6 (10), p.e487-e487
Main Authors:	Haider, M, Elala, Y C, Gangat, N, Hanson, C A, Tefferi, A
Format:	Article
Language:	English
Subjects:	Adult Aged Aged, 80 and over Disease Progression Female Follow-Up Studies Genetic Predisposition to Disease Humans Letter to the Editor Male Middle Aged Mutation Palpation Primary Myelofibrosis - diagnosis Primary Myelofibrosis - genetics Primary Myelofibrosis - pathology Prognosis Receptors, Thrombopoietin - genetics Risk Factors Splenomegaly - complications Splenomegaly - diagnosis Splenomegaly - genetics Thrombocythemia, Essential - complications Thrombocythemia, Essential - genetics Thrombocythemia, Essential - pathology
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