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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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. / Lanke, Elsa; Johansson, Anna; Halldén, Christer; Lethagen, Stefan.

In: Journal of Thrombosis and Haemostasis, Vol. 3, No. 12, 2005, p. 2656-2663.

Research output: Contribution to journalArticle

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TY - JOUR

T1 - 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.

AU - Lanke, Elsa

AU - Johansson, Anna

AU - Halldén, Christer

AU - Lethagen, Stefan

N1 - 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)

PY - 2005

Y1 - 2005

U2 - 10.1111/j.1538-7836.2005.01631.x

DO - 10.1111/j.1538-7836.2005.01631.x

M3 - Article

VL - 3

SP - 2656

EP - 2663

JO - Journal of Thrombosis and Haemostasis

T2 - Journal of Thrombosis and Haemostasis

JF - Journal of Thrombosis and Haemostasis

SN - 1538-7933

IS - 12

ER -