Associated Papers
Protein C deficiency with recurrent systemic thrombosis associated with compound heterozygous PROC missense variants.
Shiba M et al.
American Heart Journal Plus : Cardiology Research and Practice, 2025
Molecular basis of inherited protein C deficiency results from genetic variations in the signal peptide and propeptide regions.
Cao Q et al.
Journal of Thrombosis and Haemostasis : Jth, 2023
Evaluation of prothrombotic risk of two PROC hotspot mutations (Arg189Trp and Lys193del) in Chinese population: a retrospective study.
Li L et al.
Thrombosis Journal, 2023
37789321 (PubMed )
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