Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference31 articles.
1. Congenital fibrinogen disorders: an update;de Moerloose;Semin. Thromb. Hemost.,2013
2. Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion;J.A.;Proc. Natl. Acad. Sci. U. S. A.,1985
3. The covalent structure of human fibrinogen;Doolittle,1979
4. Recommendations for nomenclature on fibrinogen and fibrin;Medved;J. Thromb. Haemost.,2009
5. Structural organization of the fibrin(ogen) αC-domain;Tsurupa;Biochemistry,2002
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