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.

• Author: Elsa Lanke; Anna Johansson; Christer Halldén; Stefan Lethagen
• Department/s: Clinical Coagulation, Malmö; Department of Biology; Clinical Chemistry, Malmö; Department of Clinical Sciences, Malmö
• Publishing year: 2005
• Language: English
• Pages: 2656-2663
• Publication/Series: Journal of Thrombosis and Haemostasis
• Volume: 3
• Issue: 12
• Full text: - 274 kB; Download statistics
• Links: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16359504&dopt=Abstract; http://dx.doi.org/10.1111/j.1538-7836.2005.01631.x
• Document type: Journal article
• Publisher: Wiley-Blackwell
• Topic: Cardiac and Cardiovascular Systems
• Status: Published
• Research group: Clinical Coagulation, Malmö; Clinical Chemistry, Malmö
• ISBN/ISSN/Other: ISSN: 1538-7933