Autor/in Ala, F 1 Budde, U 1 Enayat, M S 1 Jazebi, M 1 Obser, T 1 Rassoulzadegan, M Ravanbod, S 1 Schneppenheim, R Schneppenheim, S 1 alle zeigenListe einklappen
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 Enayat, M S Ravanbod, S Rassoulzadegan, M Jazebi, M Ala, F Budde, U Schneppenheim, S 2013 - Forschungsinformationssystem des UKE
