Comparison of the Mutational Profiles of Primary Myelofibrosis, Polycythemia Vera, and Essential Thrombocytosis.

These findings indicate the special roles ASXL1 and SRSF2 may play in PMF and potential diagnostic utility of mutations in these genes in resolving the differential diagnosis. Several other genes appeared to have different mutation rates in these three entities but did not reach statistical significance, which could be due to inadequate sample numbers in this study Table 5 .

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