Title : Discrepancy between IIA phenotype and IIB genotype in a patient with a variant of von Willebrand disease.

Pub. Date : 1994 Feb 1

PMID : 8298143






1 Functional Relationships(s)
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Protein Name
Organism
1 This mutation is localized within a 509-695 disulphide loop of the vWF that plays an important role in the binding to GPIb and is where most of the molecular defects described so far were associated with type-IIB vWD. disulphide von Willebrand factor Homo sapiens