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
Genotyping of five Pakistani patients with severe inherited factor X deficiency: identification of two novel mutations.
Borhany M et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2018
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