Two cases of von Willebrand disease type 3 in consanguineousChinese families
PMID: 31793247
Gene: VMF
HGNCID: HGNC:12726
Two cases of von Willebrand disease type 3 in consanguineousChinese families
PMID: 31793247
Gene: VMF
HGNCID: HGNC:12726
A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies
PMID: 35328514 Gene: VWF HGNCID: HGNC:12726