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

Research output: Contribution to journalMeeting abstract (Journal)

Original languageEnglish
Pages (from-to)14
Number of pages <span style="color:red"p> <font size="1.5"> ✽ </span> </font>1
JournalBelgian Journal of Hematology
Volume4
Publication statusPublished - 2016
Event23rd Annual Meeting of the Belgian Society on Thrombosis and Haemostasis - Mechelen, Belgium
Duration: 19 Nov 201520 Nov 2015

Cite this