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.
Research output: Contribution to journal › Article
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Journal||Journal of Thrombosis and Haemostasis|
|Publication status||Published - 2005|
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Clinical Coagulation Research Unit (013242510), Clinical Chemistry, Malmö (013016000), Department of Cell and Organism Biology (Closed 2011.) (011002100), Emergency medicine/Medicine/Surgery (013240200)
No data available
Related research output
2008, Department of Clinical Sciences, Lund University. 105 p.
Research output: Thesis › Doctoral Thesis (compilation)