A patient with von Willebrand’s disease characterized by a compound heterozygosity for a substitution of Arg854 by Gin in the putative factor-VUI-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF allele - Peerlinck, K; Eikenboom, JC; Ploos van Amstel, HK; Sangtawesin, W; Amout, J; Reitsma, PH; Vermylen, J; Briet, E (Br J Haematol, 1992)