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Mutation status of essential thrombocythemia and primary myelofibrosis defines clinical outcome

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Bibliographic Details
Published in:	Haematologica (Roma) 2016-04, Vol.101 (4), p.e129-e132
Main Authors:	Asp, Julia, Andréasson, Björn, Hansson, Ulrika, Wasslavik, Carina, Abelsson, Johanna, Johansson, Peter, Palmqvist, Lars
Format:	Article
Language:	English
Subjects:	CALR Calreticulin - genetics Calreticulin - metabolism Clinical Laboratory Medicine DNA Mutational Analysis Gene Expression Hematologi Hematology Humans JAK2 Janus Kinase 2 - genetics Janus Kinase 2 - metabolism Klinisk laboratoriemedicin Medical Genetics Medicinsk genetik MPL Mutation Online Only PMF Primary Myelofibrosis - diagnosis Primary Myelofibrosis - genetics Primary Myelofibrosis - mortality Primary Myelofibrosis - pathology Prognosis Receptors, Thrombopoietin - genetics Receptors, Thrombopoietin - metabolism Survival Analysis Thrombocythemia, Essential - diagnosis Thrombocythemia, Essential - genetics Thrombocythemia, Essential - mortality Thrombocythemia, Essential - pathology
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