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The presence of ASXL1 mutations as well as a total number of myeloid driver mutations higher than two is strongly associated with the diagnosis of primary myelofibrosis as opposed to essential thrombocythemia 133

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The presence of ASXL1 mutations as well as a total number of myeloid driver mutations higher than two is strongly associated with the diagnosis of primary myelofibrosis as opposed to essential thrombocythemia 13 10 5 8 4 15 5

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