Open AccessClinical Research: Treatment with Warfarin Followed By Hydroxyurea for Thrombosis Caused By JAK2V617F-Positive Essential Thrombocythemia Associated with Mutation in the Thrombomodulin Gene and Deficiency of Protein S
Author(s) -
Xingfu Sun,
Jianxin Fu,
Jianyong Li,
Hua Lu
Publication year - 2020
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood-2020-136087
Subject(s) - thrombomodulin , missense mutation , thrombosis , medicine , essential thrombocythemia , mutation , gene mutation , protein c , protein s deficiency , compound heterozygosity , microbiology and biotechnology , biology , gastroenterology , pathology , platelet , protein s , genetics , gene , thrombin
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