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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family.
Levrat, Emmanuel; Aboukhamis, Imad; de Moerloose, Philippe; Farho, Jaafar; Chamaa, Sahar; Reber, Guido; Fort, Alexandre; Neerman-Arbez, Marguerite.
Affiliation
  • Levrat E; Division of Angiology and Haemostasis, University Hospital, Geneva, Switzerland.
Blood Coagul Fibrinolysis ; 22(2): 148-50, 2011 Mar.
Article in En | MEDLINE | ID: mdl-21245743
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Full text: 1 Database: MEDLINE Main subject: Fibrinogen / Frameshift Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Asia Language: En Year: 2011 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Fibrinogen / Frameshift Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Asia Language: En Year: 2011 Type: Article