Associated Papers
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family.
Zhang X et al.
International Journal of Hematology, 2020
Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins.
Nagaya S et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2018
A novel Ala275Val mutation in factor X gene influences its structural compatibility and impairs intracellular trafficking and coagulant activity.
Sun N et al.
Thrombosis Research, 2016
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