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.

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Bibtex

@article{d396e960add743fbaf1fc55bf2b24771,
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.",
author = "Elsa Lanke and Anna Johansson and Christer Halld{\'e}n and Stefan Lethagen",
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, Malm{\"o} (013016000), Department of Cell and Organism Biology (Closed 2011.) (011002100), Emergency medicine/Medicine/Surgery (013240200)",
year = "2005",
doi = "10.1111/j.1538-7836.2005.01631.x",
language = "English",
volume = "3",
pages = "2656--2663",
journal = "Journal of Thrombosis and Haemostasis",
issn = "1538-7933",
publisher = "Federation of European Neuroscience Societies and Blackwell Publishing Ltd",
number = "12",

}