Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family

Publisher: John Wiley & Sons Inc

E-ISSN: 1365-2516|21|6|846-851

ISSN: 1351-8216

Source: HAEMOPHILIA, Vol.21, Iss.6, 2015-11, pp. : 846-851

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Abstract