✦ LIBER ✦
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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