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
Five new F10 variants in hereditary factor x deficiency detected by high-throughput sequencing.
Pastoret C et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2023
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
Factor X M402T: a homozygous missense mutation identified as the cause of cross-reacting material-reduced deficiency.
Chikasawa Y et al.
International Journal of Hematology, 2014
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran.
Karimi M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2012
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
Molecular basis of factor X deficiency cases from India.
Mota L et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2010
Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency.
Karimi M et al.
Haematologica, 2008
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