A Database for Human Fibrinogen Variants
- 1 June 2001
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 936 (1), 89-90
- https://doi.org/10.1111/j.1749-6632.2001.tb03495.x
Abstract
Identifying and studying abnormal human fibrinogens is a source of much information, and helps in taking care of the affected patients. To permit exhaustive numbering and easy updates, an extensive register has been compiled and made available on the internet. Known molecular abnormalities are mentioned with the essential clinical features.Keywords
This publication has 4 references indexed in Scilit:
- Structure and function of fibrinogen inferred from hereditary dysfibrinogensFibrinolysis and Proteolysis, 2000
- Dysfibrinogenemia and ThrombosisSeminars in Thrombosis and Hemostasis, 1999
- γ-Chain Dysfibrinogenemias: Molecular Structure-Function Relationships of Naturally Occurring Mutations in the γ Chain of Human FibrinogenBlood, 1998
- Familial Dysfibrinogenemia and ThrombophiliaThrombosis and Haemostasis, 1995