Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residues
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2003.00435.x/fullpdf
Reference26 articles.
1. BIOCHEMISTRY AND GENETICS OF VON WILLEBRAND FACTOR
2. Identification of disulfide-bridged substructures within human von Willebrand factor
3. A Revised Classification of von Willebrand Disease
4. Molecular Genetics of von Willebrand Disease
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3. VWF‐Gly2752Ser, a novel non‐cysteine substitution variant in the CK domain, exhibits severe secretory impairment by hampering C‐terminal dimer formation;Journal of Thrombosis and Haemostasis;2022-08
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