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 › ST3.5
Distinctive regional-specific PROS1 mutation spectrum in Southern China.
Chan NCN et al.
Journal of Thrombosis and Thrombolysis, 2018
Genotype and laboratory and clinical phenotypes of protein s deficiency.
Duebgen S et al.
American Journal of Clinical Pathology, 2012
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