DOI:
10.1055/s-00034925
Hämostaseologie
LinksClose Window
References
Vettore S, Scandellari R, Moro S. et al.
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant.
Haematologica 2008;
93 (11) 1743-1747
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.