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JAK2V617F mutation as a marker of a latent myeloproliferative disorder in a patient with Budd-Chiari syndrome and factor V Leiden mutation.

作者信息

Plumé Gema, Vayá Amparo, Ferrando Fernando, Mira Yolanda, Orbis Francisco

机构信息

Thrombosis and Hemostasis Unit, Department of Clinical Pathology, La Fe University Hospital, Valencia, Spain.

出版信息

Thromb Haemost. 2007 Sep;98(3):681-2.

PMID:17849060
Abstract
摘要

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JAK2V617F mutation as a marker of a latent myeloproliferative disorder in a patient with Budd-Chiari syndrome and factor V Leiden mutation.JAK2V617F突变作为布加综合征合并因子V莱顿突变患者潜在骨髓增殖性疾病的标志物。
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引用本文的文献

1
Budd-Chiari Syndrome in a Patient with JAK-2 V617F and Factor V G1691A Mutations.一名患有JAK-2 V617F和凝血因子V G1691A突变的患者的布加综合征
West Indian Med J. 2014 Sep;63(5):528-31. doi: 10.7727/wimj.2013.228. Epub 2014 Jun 10.
2
The clinical significance of JAK2V617F mutation for Philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis.JAK2V617F 突变对伴有门脉系统血栓形成的非费城染色体阴性慢性骨髓增殖性肿瘤患者的临床意义。
J Thromb Thrombolysis. 2012 Oct;34(3):388-96. doi: 10.1007/s11239-012-0738-2.
3
Etiology and portal vein thrombosis in Budd-Chiari syndrome.
布加综合征的病因及门静脉血栓形成
World J Gastroenterol. 2008 May 14;14(18):2858-62. doi: 10.3748/wjg.14.2858.