Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia. [electronic resource]

By: Contributor(s): Producer: 20170324Description: 455-8 p. digitalISSN:
  • 1098-9064
Subject(s): Online resources: In: Seminars in thrombosis and hemostasis vol. 42
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Publication Type: Letter

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