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References
These sources were used to develop the Genetics Home Reference
gene summary
on the
FGB
gene.
Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML. Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood. 2000 Feb 15;95(4):1336-41.
PubMed citation
Entrez
Gene
Neerman-Arbez M. Molecular basis of fibrinogen deficiency. Pathophysiol Haemost Thromb. 2006;35(1-2):187-98. Review.
PubMed citation
OMIM:
FIBRINOGEN, B BETA
POLYPEPTIDE
Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M. Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia. Hum Mol Genet. 2005 Nov 1;14(21):3271-80. Epub 2005 Sep 29.
PubMed citation
Weisel JW. Fibrinogen and fibrin. Adv Protein Chem. 2005;70:247-99. Review.
PubMed citation
Reviewed: February 2012
Published: June 17, 2013
Indicates a page outside Genetics Home Reference.