DOI:
10.1055/s-00033990
TH Open
LinksClose Window
References
Lethagen S, Isaksson C, Schaedel C, Holmberg L.
Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).
Thromb Haemost 2002;
88 (03) 421-426
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.