Articles

PP2.3 A novel FGA mutation underlying a case of congenital dysfibrinogenemia with unusual clinical presentation

BJH - volume 7, issue Abstract Book BHS, january 2016

M. Tajdar PharmD, M. Herpol , C. Orlando , B. De Bisschop , P. Govaert , K. Jochmans MD, PhD

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A novel FGA mutation underlying a case of congenital dysfibrinogenemia with unusual clinical presentation

BJH - volume 6, issue Abstract Book BSTH, november 2015

M. Tajdar PharmD, M. Herpol , C. Orlando , B. De Bisschop , P. Govaert , K. Jochmans MD, PhD

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