Novel fibrinogen (Bβ401Gly→Val) presents as dys- or hypodysfibrinogenaemia due to alterations in sialic acid content
Author:
Publisher
Georg Thieme Verlag KG
Subject
Hematology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH11-05-0287.pdf
Reference15 articles.
1. Human plasma fibrinogen is synthesized in the liver
2. The Role of βγ and αγ Complexes in the Assembly of Human Fibrinogen
3. Carbohydrate structure of human fibrinogen. Use of 300-MHz 1H-NMR to characterize glycosidase-treated glycopeptides.
4. The role of sialic acid in the dysfibrinogenemia associated with liver disease: distribution of sialic acid on the constituent chains
5. Dysfibrinogenemia Associated with Hepatoma
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2. Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder;International Journal of Molecular Sciences;2022-01-10
3. Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations;Thrombosis Research;2021-01
4. Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation;Journal of Thrombosis and Haemostasis;2017-03-06
5. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders;Seminars in Thrombosis and Hemostasis;2016-03-28
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