Ph阴性经典骨髓增殖性肿瘤：关键概念和欧洲白血病网的治疗建议
摘要
1引言
超过90％的真性红细胞增多症（polycythemia vera，PV）和60％左右的原发性血小板增多症（essential thrombocythemia，ET）或原发性骨髓纤维化（primary myelofibrosis，PMF）患者蛋白酪氨酸激酶JAK2存在突变（V617F），这一发现改变了我们对Ph阴性经典骨髓增殖性肿瘤（myeloproliferative neoplasms，
出处
《国际输血及血液学杂志》
CAS
2011年第3期274-277,共4页
International Journal of Blood Transfusion and Hematology
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