Two cases of von Willebrand disease type 3 in consanguineous Chinese families

Abstract Background von Willebrand disease (VWD) is the most common inherited bleeding disorder caused by defective or deficient von Willebrand factor (VWF). VWD type 3 is inherited in autosomal recessive manner. We described clinical and molecular features of VWD type 3 in two consanguineous marria...

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Bibliographic Details
Main Authors: Xiong Wang, Ning Tang, Yanjun Lu, Qun Hu, Dengju Li
Format: Article
Language:English
Published: Wiley 2020-02-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
Online Access:https://doi.org/10.1002/mgg3.1075