Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference18 articles.
1. Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families;Dorgalaleh;Blood Coagul Fibrinolysis,2019
2. A novel mutation (Tyr503Cys) in a severe factor XI deficiency;Su;Blood Coagul Fibrinolysis,2018
3. Recent advances in the discovery and development of factor XI/XIa inhibitors;Al-Horani;Med Res Rev,2018
4. The hemostatic role of factor XI;Puy;Thromb Res,2016
5. New hemophilia-like disease caused by deficiency of a third plasma thromboplastin factor;Rosenthal;Proc Soc Exp Biol Med,1953
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