Article
Effects of the mutant von Willebrand factor gene in von Willebrand disease.
Human genetics - 1 Oct 1995
Zhang Z, Lindstedt M, Blombäck M, Anvret M
Abstract excerpt
Von Willebrand disease (vWD) is a common inherited bleeding disorder in humans, and can be divided into a mild (type 1) and severe (type 3) form. Previous linkage studies identified one subject with vWD type 1 who transmitted different alleles of the von Willebrand factor (vWF) gene to his two af...
Topics
- Adult
- Aged
- Aged, 80 and over
- Alleles
- Base Sequence
- Exons
- Female
- Genotype
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymerase Chain Reaction
- von Willebrand Diseases
- von Willebrand Factor