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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2020-02-01
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Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.1075 |