Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations(γAla341Thr, Bβ Tyr326Cys and Aα Asp496Asn) - Hanss, Michel; Chevreaud, Caroline; French, Patrick; Négrier, Claude; Mazancourt, Philippe de (Thrombosis and Haemostasis, 2007)