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.
作者信息
Enayat M S, Ravanbod S, Rassoulzadegan M, Jazebi M, Ala F, Budde U, Schneppenheim S, Obser T, Schneppenheim R
出版信息
Haemophilia. 2013 Jul;19(4):e261-4. doi: 10.1111/hae.12161. Epub 2013 May 7.
PMID:23647747
Abstract
摘要
Zotero 插件