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
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis.
Preisler B et al.
Journal of Clinical Medicine, 2021
The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation.
Girolami A et al.
British Journal of Haematology, 2020
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.
Girolami A et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2018
Congenital combined deficiency of coagulation factors VII and X--different genetic mechanisms.
Pavlova A et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2015
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