Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference31 articles.
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1. Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency;Annals of Hematology;2023-11-10
2. Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review;Medicine;2022-10-21
3. Pathogenic variants of PROC gene caused type I activity deficiency in a familial Chinese venous thrombosis;Journal of Cellular and Molecular Medicine;2019-07-23
4. Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes;Thrombosis Research;2016-09
5. Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations;Gene;2015-05
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