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首页> 外文期刊>Haematologica >Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis | Haematologica
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Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis | Haematologica

机译:在世卫组织临时实体中发生jak2 v617f突变:髓细胞增生/肌酚抗原疾病,与标记血小板症相关的圆形膀胱细胞的无分配 - 难治性贫血哈及炎

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摘要

The JAK2/V617F mutation has been noted in essential thrombocytemia. We investigated 19 cases with refractory anemia with ringed sideroblasts (RARS), including three RARS with thrombocytosis (RARS-T). Only the RARS-T patients showed this mutation. More cases need to be analyzed to determine the prevalence of the JAK2/V617F mutation in RARS-T.
机译:jak2 / v617f突变已在必要的血小板血症中发现。我们调查了19例耐火性贫血,带有戒指的血管血细胞(RARS),其中包括三种血小板症(RARS-T)。只有RARS-T患者才显示出这种突变。需要分析更多案例以确定RARS-T中JAK2 / V617F突变的患病率。

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