LUP Statistics
Record
- Title
- Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype.
- Type
- Journal Article
- Publ. year
- 2005
- Author/s
- Lanke, Elsa; Johansson, Anna; Halldén, Christer; Lethagen, Stefan
- Department/s
- Clinical Coagulation, Malmö; Department of Biology; Clinical Chemistry, Malmö; Department of Clinical Sciences, Malmö
- In LUP since
- 2016-04-01
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