Associated Papers
Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese Pedigree.
Feng Y et al.
Genes, 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
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