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

Onderzoeksoutput: Meeting abstract (Journal)

Originele taal-2English
Pagina's (van-tot)14
Aantal pagina's1
TijdschriftBelgian Journal of Hematology
Volume4
StatusPublished - 2016
Evenement23rd Annual Meeting of the Belgian Society on Thrombosis and Haemostasis - Mechelen, Belgium
Duur: 19 nov 201520 nov 2015

Citeer dit