A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PSα (PROS1)
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/19/18/5091/3760450/19-18-5091a.pdf
Cited by 29 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Thrombin generation as an intermediate phenotype for venous thrombosis;Thrombosis and Haemostasis;2010
2. Single nucleotide polymorphisms and haplotypes of protein C and protein S genes in the Thai population;Blood Coagulation & Fibrinolysis;2006-01
3. The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population;British Journal of Haematology;2004-04-27
4. Superior Mesenteric Venous Thrombosis Associated With a Familial Missense Mutation (Pro626Leu) in the SHBG-Like Domain of the Protein S Molecule;International Journal of Hematology;2002-01
5. A Novel Splice Acceptor Site Mutation of Protein S Gene in Affected Individuals with Type I Protein S Deficiency: Allelic Exclusion of the Mutant Gene;Thrombosis Research;2001-03
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