PB0209 Clinical Manifestations of Patients with Congenital Dysfibrinogenemia with the Most Common Hotspot Mutation in FGA Gene p.Arg35His

Autor:	Simurda, T., Drotarova, M., Zolkova, J., Kolkova, Z., Loderer, D., Skornova, I., Brunclikova, M., Grendar, M., Lasabova, Z., Stasko, J., Kubisz, P.
Zdroj:	In Research and Practice in Thrombosis and Haemostasis October 2023 7 Supplement 2
Databáze:	ScienceDirect
Externí odkaz:	Plný text