Associated Papers
Molecular Aspects of Rare Coagulation Factor Deficiencies.
Tourbih H et al.
Cureus, 2025
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
Occurrence and management of severe bleeding episodes in patients with hereditary factor X deficiency.
Tarantino MD
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2021
Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.
Togashi T et al.
International Journal of Hematology, 2020
Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage.
Matsuo Y et al.
The Kurume Medical Journal, 2017
Select a paper to view details