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

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 marriage famil...

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Detalles Bibliográficos
Autores principales: Wang, Xiong, Tang, Ning, Lu, Yanjun, Hu, Qun, Li, Dengju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005608/
https://www.ncbi.nlm.nih.gov/pubmed/31793247
http://dx.doi.org/10.1002/mgg3.1075

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005608/
https://www.ncbi.nlm.nih.gov/pubmed/31793247
http://dx.doi.org/10.1002/mgg3.1075

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