SERPINC1 novel mutation (c.637C > T p. Gln213Ter) in a cerebral venous sinus thrombosis case and treatment with agatroban
Author:
Funder
Natural Science Foundation of Beijing Municipality
Beijing Municipal Science and Technology Commission
Publisher
Elsevier BV
Subject
Hematology
Reference10 articles.
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3. Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency;Luxembourg;Thromb. Haemost.,2014
4. A novel splice-site mutation c.42-2A>T (IVS1-2A>T) of SERPINC1 in a Korean family with inherited antithrombin deficiency;Jang;Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis.,2011
5. Rare double heterozygous mutations in antithrombin underlie hereditary thrombophilia in a Chinese family;Deng;J. Thromb. Thrombolysis,2013
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1. Argatroban Resistance and Successful Adjunctive Anticoagulation for Cerebral Venous Sinus Thrombosis With SERPINC1 Mutation;Neurology Clinical Practice;2023-04
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