Article
Variation in the VWF gene in Swedish patients with type 1 von Willebrand Disease.
Annals of human genetics - 1 Jul 2011
Johansson Anna M, Halldén Christer, Säll Torbjörn, Lethagen Stefan
Abstract excerpt
The spectrum of mutations in the von Willebrand factor (VWF) gene in a Swedish type 1 von Willebrand disease (VWD) population was investigated. To gain more knowledge about the dynamics of VWD mutations, the data were analyzed from a population genetics perspective. The VWF gene was resequenced in 54 Swedish patients diagnosed with type 1 VWD. Fifty-five variable sites were located in exons, 10 in the promoter...
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