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For: Ding Q, Shen W, Ye X, Wu Y, Wang X, Wang H. Clinical and genetic features of protein C deficiency in 23 unrelated Chinese patients. Blood Cells, Molecules, and Diseases 2013;50:53-8. [DOI: 10.1016/j.bcmd.2012.08.004] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Su K, Zhang H, Fang W, Zhang F, Yang L, Jin Y, Wang M. Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis. Blood Coagul Fibrinolysis 2018;29:714-9. [PMID: 30439769 DOI: 10.1097/MBC.0000000000000778] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Su K, Wang L, Wang M, Wang H. A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency. Blood Coagul Fibrinolysis 2021;32:140-5. [PMID: 33443922 DOI: 10.1097/MBC.0000000000001003] [Reference Citation Analysis]
3 Shen W, Gu Y, Zhu R, Zhang L, Zhang J, Ying C. Copy number variations of the F8 gene are associated with venous thromboembolism. Blood Cells, Molecules, and Diseases 2013;50:259-62. [DOI: 10.1016/j.bcmd.2013.01.004] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.7] [Reference Citation Analysis]
4 Zhang YP, Lin B, Ji YY, Hu YN, Lin XF, Tang Y, Zhang JH, Wu SJ, Cai SL, Zhou YF, Chen T, Fang ZT, Luo JW. A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1. Thromb J 2021;19:64. [PMID: 34496879 DOI: 10.1186/s12959-021-00316-4] [Reference Citation Analysis]
5 Wu X, Li L, Ding Q, Wang X, Wu F, Wu W. Screening and functional exploration of prothrombin Arg596 related mutations in Chinese venous thromboembolism patients. J Clin Pathol 2018;71:614-9. [PMID: 29331940 DOI: 10.1136/jclinpath-2017-204888] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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9 Luan CJ, Shen W, Yu Z, Chen L, Gu Y, Tang LY, Wang ZG, Dai L, Gu MM. Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay. Thromb Res 2015;135:733-8. [PMID: 25648792 DOI: 10.1016/j.thromres.2015.01.022] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
10 Ding Q, Yang L, Hassanian SM, Rezaie AR. Expression and functional characterisation of natural R147W and K150del variants of protein C in the Chinese population. Thromb Haemost 2013;109:614-24. [PMID: 23389250 DOI: 10.1160/TH12-10-0760] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]
11 Sun L, Li X, Li Q, Wang L, Li J, Shu C. Multiple arterial and venous thromboembolism in a male patient with hereditary protein C deficiency: A case report. Medicine (Baltimore) 2021;100:e25575. [PMID: 33847687 DOI: 10.1097/MD.0000000000025575] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Zhao L, Li C, Shao R, Fang Y. Risk indicators for venous thrombosis in first-degree relatives of patients with recurrent venous thromboembolism in Chinese. Medicine (Baltimore) 2016;95:e4539. [PMID: 27741098 DOI: 10.1097/MD.0000000000004539] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]