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

By: Contributor(s): Producer: 20160809Description: 846-51 p. digitalISSN:
  • 1365-2516
Subject(s): Online resources: In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 21
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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