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钙网蛋白基因突变的原发性血小板增多症二例并文献复习 被引量:3

Essential thrombocytosis with calreticulin gene mutation: report of two cases and review of literature
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摘要 目的探讨钙网蛋白(CALR)基因在原发性血小板增多症(ET)诊断中的临床价值。方法分析2例CALR基因突变的ET病例,并进行相关文献复习。结果结合实验室检查、骨髓检查及CALR基因阳性结果,2例患者明确诊断为ET,给予阿司匹林联合干扰素α治疗,病情稳定。结论CALR基因在JAK2阴性的ET中具有重要的诊断价值,值得临床推广。
出处 《肿瘤研究与临床》 CAS 2018年第2期132-134,共3页 Cancer Research and Clinic
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