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5. Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens. Kotlín R; Blažek B; Suttnar J; Malý M; Kvasnička J; Dyr JE Blood Coagul Fibrinolysis; 2010 Oct; 21(7):640-8. PubMed ID: 20829681 [TBL] [Abstract][Full Text] [Related]
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20. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia. Marchi R; Brennan S; Meyer M; Rojas H; Kanzler D; De Agrela M; Ruiz-Saez A Blood Cells Mol Dis; 2013 Mar; 50(3):177-81. PubMed ID: 23266225 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]