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bibliographicCitation Tefferi A, Lasho TL, Hanson CA, Ketterling RP, Gangat N, Pardanani A. Screening for ASXL1 and SRSF2 mutations is imperative for treatment decision‐making in otherwise low or intermediate‐1 risk patients with myelofibrosis. Br J Haematol. 2017 Nov 23;183(4):678–81. doi: 10.1111/bjh.15010.
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title Screening for ASXL1 and SRSF2 mutations is imperative for treatment decision‐making in otherwise low or intermediate‐1 risk patients with myelofibrosis
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