Epigenetic, polymorphic and mutational (Αα167Arg→Lys) contribution to a functionally abnormal fibrinogen
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2011.04337.x/fullpdf
Reference13 articles.
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3. Substitution (γ335Trp→Arg) in fibrinogen Fremantle causes diminished γ chain expression and increased sialic acid content;Brennan;Thromb Haemost,2010
4. The role of sialic acid in the dysfibrinogenima associated with liver disease, distribution of sialic acid on the constituent chains;Martinez;Blood,1983
5. Valproate-associated coagulopathies in children during short-term treatment;Kose;J Child Neurol,2009
Cited by 2 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. Novel FGG variant (ү339C→S) confirms importance of the ү326–339 disulphide bond for plasma expression of newly synthesised fibrinogen;Thrombosis and Haemostasis;2015-07
2. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia;Blood Cells, Molecules, and Diseases;2013-03
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