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
Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation.
Bicocchi MP et al.
European Journal of Haematology, 2013
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