Medical Knowledge Cockpit afibrinogenemia, congenital

• Complement and coagulation cascades
  Homo sapiens (human) 2 genes

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FGA

• Platelet-fibrinogen interactions
• Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion
• Structure and function of human fibrinogen inferred from dysfibrinogens

FGB

• A new congenital abnormal fibrinogen Ise characterized by the replacement of B beta glycine-15 by cysteine.
• Nucleotide sequences of the three genes coding for human fibrinogen.
• Intracellular fate of fibrinogen B beta chain expressed in COS cells.