Molecular basis of inherited protein C deficiency results from genetic variations in the signal peptide and propeptide regions-Reference-Cited by-同舟云学术

Molecular basis of inherited protein C deficiency results from genetic variations in the signal peptide and propeptide regions

Published:2023-11 Issue:11 Volume:21 Page:3124-3137
ISSN:1538-7836
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:Journal of Thrombosis and Haemostasis

Author:

Cao Qing,Hao Zhenyu,Li Cheng,Chen Xuejie,Gao Meng,Jiang Nan,Liu Hongli,Shen Yan,Yang Haiping,Zhang Shujuan,Yang Aiying,Li Weikai,Tie Jian-Ke,Shen Guomin

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Department of Science and Technology, Ministry of Science and Technology, India

National Institutes of Health

Publisher

Elsevier BV

Subject

Hematology

Reference30 articles.

1. Protein C deficiency;Dinarvand;Arch Pathol Lab Med,2019

2. Protein C deficiency;Goldenberg;Haemophilia,2008

3. A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin;Mahmoodi;J Thromb Haemost,2010

4. Molecular genetic analysis of severe protein C deficiency;Millar;Hum Genet,2000

5. Diagnosis and management of severe congenital protein C deficiency (SCPCD): communication from the SSC of the ISTH;Minford;J Thromb Haemost,2022

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