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
Coagulation factor X Arg386 specifically affects activation by the intrinsic pathway: a novel patient mutation.
Vanden Hoek AL et al.
Journal of Thrombosis and Haemostasis : Jth, 2012
Molecular characterization of two novel mutations causing factor X deficiency in a Chinese pedigree.
Wang WB et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2005
[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].
Fu QH et al.
Zhonghua Yi Xue Za Zhi, 2003
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