𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Different organization of von Willebrand factor oligomers in type-2A and -2B von Willebrand disease variants: effects of DDAVP infusion and protease inhibitors

✍ Scribed by A. Casonato; E. Pontara; A. Bertomoro; D. Dannhauser; S. Secchiero; M. Zaninotto; A. Girolami


Publisher
Springer
Year
1995
Tongue
English
Weight
883 KB
Volume
71
Category
Article
ISSN
0939-5555

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Search for mutations in a segment of the
✍ CasaΓ±a, Pilar; MartΓ­nez, Francisco; EspinΓ³s, Carmen; Haya, Saturnino; Lorenzo, J πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 431 KB πŸ‘ 1 views

von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which