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Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report
Eun Jin Cho, Yong Chul Kim, Jin Ho Hwang, Hajung Lee, Sung Sup Park, So Yeon Kim, Suhnggwon Kim, Ho Jun Chin
Kidney Res Clin Pract. 2012;31(1):72-75.   Published online January 18, 2012
DOI: https://doi.org/10.1016/j.krcp.2011.12.003

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Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report
Kidney Research and Clinical Practice. 2012;31(1):72-75   Crossref logo
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Severe arterial thrombosis in a family with type III protein S deficiency caused by a frameshift mutation in the PROS1 gene
Thrombosis Research. 2010;126(2):e159-e161   Crossref logo
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One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis
American Journal of Hematology. 2006;81(10):787-797   Crossref logo
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Inherited protein S deficiency as a reszult of a large duplication mutation of thePROS1gene detected by multiplex ligation-dependent probe amplification
Journal of Thrombosis and Haemostasis. 2008;6(8):1430-1432   Crossref logo
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Portal-Splenic-Mesenteric Venous Thrombosis in a Patients with Protein S Deficiency due to NovelPROS1Gene Mutation
The Korean Journal of Gastroenterology. 2014;64(2):110   Crossref logo
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Three case reports of inherited antithrombin deficiency in China: double novel missense mutations, a nonsense mutation and a frameshift mutation
Journal of Thrombosis and Thrombolysis. 2012;34(2):244-250   Crossref logo
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Protein S inherited qualitative deficiency: novel mutations and phenotypic influence
Journal of Thrombosis and Haemostasis. 2010;8(12):2718-2726   Crossref logo
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Venous thromboembolism associated with protein S deficiency due to $$\hbox {Arg}451^{*}$$ Arg 451 ∗ mutation in PROS1 gene: a case report and a literature review
Journal of Genetics. 2017;96(6):1047-1051   Crossref logo
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A novel splicing mutation in the PROS1 gene causes hereditary protein S deficiency in a Chinese family with thrombotic disease
Thrombosis Research. 2020;189:93-95   Crossref logo
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Inherited Antithrombin III Deficiency: A Case Report of Familial Pedigree and Gene Mutation Screening
European Journal of Vascular and Endovascular Surgery. 2019;58(6):e379   Crossref logo
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