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 journalArticle

Details

Authors
  • Elsa Lanke
  • Anna Johansson
  • Christer Halldén
  • Stefan Lethagen
Organisations
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Cardiac and Cardiovascular Systems
Original languageEnglish
Pages (from-to)2656-2663
JournalJournal of Thrombosis and Haemostasis
Volume3
Issue number12
Publication statusPublished - 2005
Publication categoryResearch
Peer-reviewedYes

Bibliographic note

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)

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Related research output

Lanke, E., 2008, Department of Clinical Sciences, Lund University. 105 p.

Research output: ThesisDoctoral Thesis (compilation)

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