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afibrinogenemia, congenital
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FGA
Structure and function of human fibrinogen inferred from dysfibrinogens
New insights into fibrin (ogen) structure and function
Genetic and environmental determinants of fibrin structure and function: relevance to clinical disease
FGB
Disulfide bridges in nh2 -terminal part of human fibrinogen.
Abnormal fibrinogens IJmuiden (B beta Arg14----Cys) and Nijmegen (B beta Arg44----Cys) form disulfide-linked fibrinogen-albumin complexes.
Molecular basis of fibrinogen Naples associated with defective thrombin binding and thrombophilia. Homozygous substitution of B beta 68 Ala----Thr.
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Complement and coagulation cascades
Homo sapiens (human)
2 genes
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