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A patient with von Willebrand's disease characterized by a compound heterozygosity for a substitution of Arg by Gln in the putative factor-VIII-binding domain of von Willebrand factor (vWF) on one allele and very low levels of mRNA from the second vWF allele

✍ Scribed by Kathelijne Peerlinck; Jeroen C. J. Eikenboom; Hans K. Ploos; Van Amstel; Wanida Sangtawesin; Jef Arnout; Pieter H. Reitsma; Jos Vermylen; Ernest Brieut


Book ID
114712943
Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
961 KB
Volume
80
Category
Article
ISSN
0007-1048

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