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The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor
Blood (1996) 87 (3): 1013–1021.
Blood (1992) 80 (12): 3260–3261.
Blood (1992) 80 (10): 2690–2691.
Synthetic factor VIII peptides with amino acid sequences contained within the C2 domain of factor VIII inhibit factor VIII binding to phosphatidylserine
Blood (1990) 75 (10): 1999–2004.