Associated Papers
Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review.
Zhang Z et al.
Medicine, 2022
A novel mutation c.1048A>T at codon 350(Lys>Stop) in PROC gene causing neonatal purpura fulminans.
Jain R et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2013
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