Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient. (7th May 2013) - Enayat, M. S.; Ravanbod, S.; Rassoulzadegan, M.; Jazebi, M.; Ala, F.; Budde, U.; Schneppenheim, S.; Obser, T.; Schneppenheim, R.