Absence of JAK2-V617F in paroxysmal nocturnal haemoglobinuria-associated thrombosis

被引：7
作者：
Fouassier, Marc [1 ]
Girodon, Francois [2 ]
Cleyrat, Cedric [3 ]
Robillard, Nelly
Garand, Richard
Hermouet, Sylvie [3 ]
机构：
[1] CHU Nantes, Hematol Lab, Inst Biol, F-44093 Nantes, France
[2] CHU Dijon, Hematol Lab, Dijon, France
[3] CHU Nantes, INSERM, UMR 892, Inst Biol, F-44035 Nantes 01, France
来源：
THROMBOSIS AND HAEMOSTASIS | 2009年 / 102卷 / 01期
关键词：
LATENT MYELOPROLIFERATIVE DISORDER; VEIN-THROMBOSIS; ESSENTIAL THROMBOCYTHEMIA; MYELODYSPLASTIC SYNDROMES; V617F MUTATION; JAK2; V617F; DIAGNOSIS; CLONES; DEFICIENT; ANEMIA;
D O I：
10.1160/TH09-03-0140
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：180 / 182
页数：3
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