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
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency.
Epcacan S et al.
European Journal of Clinical Investigation, 2015
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