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
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M. Jazebi | F. Ala | R. Schneppenheim | U. Budde | T. Obser | S. Schneppenheim | M. S. Enayat | S. Ravanbod | M. Rassoulzadegan | M. Enayat