Autor/in Schneppenheim, R 2 Schneppenheim, S Ala, F 1 Armstrong, E 1 Budde, U 1 Enayat, M S 1 Jazebi, M 1 Jokela, V 1 Joutsi-Korhonen, L 1 Lassila, R 1 Obser, T 1 Oyen, F 1 Rassoulzadegan, M 1 Ravanbod, S 1 Szanto, T 1 alle zeigenListe einklappen
Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations Jokela, V Lassila, R Szanto, T Joutsi-Korhonen, L Armstrong, E Oyen, F Schneppenheim, S 2013 - Forschungsinformationssystem des UKE
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