The allele frequencies at the tetranucleotide repeat (TCTA) vWA locus in the vWF gene were determined in the general Finnish population, in a population representing an internal isolate of Finland, in the Vologda-Russian population, and in US Black population samples. The allele and genotype frequen
✦ LIBER ✦
Allele frequencies of three STRs of the human von Willebrand factor gene (vWF) in a Brazilian population sample
✍ Scribed by R. C. Pagotto; M. C. T. Canas; R. O. A. A. Brito; A. L. Simões
- Publisher
- Springer-Verlag
- Year
- 1999
- Tongue
- German
- Weight
- 29 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0937-9827
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von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which