DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
LinksClose Window
References
Cai R, Li Y, Wang W. et al.
A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: a case report.
Medicine (Baltimore) 2018;
97 (40) e12697
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.