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
A Compound Heterozygosis of Two Novel Mutations Causes Factor X Deficiency in a Chinese Pedigree.
Lu S et al.
Acta Haematologica, 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
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