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

Mercedeh Tajdar, Margaux Herpol, Christelle Orlando, Barbara De Bisschop, Paul Govaert, Kristin Jochmans

Research output: Contribution to journal › Meeting abstract (Journal)

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23rd Annual Meeting of the Belgian Society on Thrombosis and Haemostasis
Christelle Orlando (Participant)
19 Nov 2015 → 20 Nov 2015
Activity: Participating in or organising an event › Participation in conference