RecName: Full=von Willebrand factor; Short=vWF; Flags: Precursor

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A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers. [Anim Genet. 2017]
A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers.
Vos-Loohuis M, van Oost BA, Dangel C, Langbein-Detsch I, Leegwater PA. Anim Genet. 2017 Aug; 48(4):493-496. Epub 2017 Feb 3.
Mutation causing von Willebrand's disease in Scottish Terriers. [J Vet Intern Med. 2000]
Mutation causing von Willebrand's disease in Scottish Terriers.
Venta PJ, Li J, Yuzbasiyan-Gurkan V, Brewer GJ, Schall WD. J Vet Intern Med. 2000 Jan-Feb; 14(1):10-9.
[Expressions of CD31 and vWF in arachnoid villus endothelium cell from experimental animal with Hydrocephalus]. [Sichuan Da Xue Xue Bao Yi Xue ...]
[Expressions of CD31 and vWF in arachnoid villus endothelium cell from experimental animal with Hydrocephalus].
Wang ER, Tang J, Sun H, Mao BY. Sichuan Da Xue Xue Bao Yi Xue Ban. 2007 Jun; 38(3):408-12.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the VWF gene.

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
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