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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.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Jul 2013

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

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PMID: 23647747
DOI: 10.1111/hae.12161

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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.PMID 23647747Read ↗

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