A patient with von Willebrand’s disease characterized by a compound heterozygosity for a substitution of Arg 854 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; Arnout, J; Reitsma, PH; Vermylen, J; Briet, E
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