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 272 Genetic Variants in the Upgraded Interactive FXI Web Database Reveals New Insights into FXI Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
The spectrum of factor XI deficiency in Italy.
Castaman G et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2014
Molecular analysis of severe factor XI deficiency in three Italian patients.
Bicocchi MP et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2011
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