Hilbert L.,1999

Hilbert L., Ruan S., Jorieux M., Fontenay-Roupie N., Stielje S., Lavergne J.M., Lavergne E., Fressinaud D., Meyer C. and the ISERM network on molecular abnormalities in vWD. - Identification of two closely located new type 2N von Willebrand disease mutations (try-32-Cys and Met-37-Val). - Thromb.Haemost., 1999, (abst. 882).

Ссылки: