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Von-Willebrand-Disease Type 1
Order number: GSD370
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Application:
- Identification of heterozygous carriers
- Differential diagnosis of coagulation disorders
Von Willebrand disease (vWD) type 1 is due to a reduction of the blood clotting factor of the same name, caused by a mutation in exon 43. The mode of inheritance is autosomal recessive, only dogs with two defective genes are affected. The effect manifests itself in...
- Identification of heterozygous carriers
- Differential diagnosis of coagulation disorders
Von Willebrand disease (vWD) type 1 is due to a reduction of the blood clotting factor of the same name, caused by a mutation in exon 43. The mode of inheritance is autosomal recessive, only dogs with two defective genes are affected. The effect manifests itself in...