Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference29 articles.
1. Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion;Redman;Ann. N. Y. Acad. Sci.,2001
2. Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion;Kant;Proc. Natl. Acad. Sci. U. S. A.,1985
3. Congenital fibrinogen disorders: an update;de Moerloose;Semin. Thromb. Hemost.,2013
4. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations;Neerman-Arbez;Hum. Mutat.,2007
5. Human fibrinogen: molecular and genetic aspects of congenital disorders;Tiscia;Int. J. Mol. Sci.,2018
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