Associated Papers
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.4
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
Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition.
Ferrarese M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019
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
Factor X deficiency and intracranial bleeding: who is at risk?
Rauch R et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2011
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