ΔC in Exon 18 of the von Willebrand Gene Is Uncommon in German vWD Type III Patients

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Thromb Haemost 1993; 70(06): 1064-1065
DOI: 10.1055/s-0038-1649727

Letter to the Editor

Schattauer GmbH Stuttgart

Authors

Günter Mertes

Dept. of Exp. Haemat. and Transf. Med., University of Bonn, Bonn, Germany
Michael Ludwig

¹Dept. of Exp. Haemat. and Transf. Med., University of Bonn, Bonn, Germany
Rainer Schwaab

Dept. of Exp. Haemat. and Transf. Med., University of Bonn, Bonn, Germany
Hans-Her-mann Brackmann

Dept. of Exp. Haemat. and Transf. Med., University of Bonn, Bonn, Germany
Klaus Olek

¹Dept. of Exp. Haemat. and Transf. Med., University of Bonn, Bonn, Germany

Received 11 June 1993

Accepted after revision 19 August 1993

Publication Date:
26 July 2018 (online)

References
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4 Zhang ZP, Falk G, Blombäck M, Egberg N, Anvret M. A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients. Hum Mol Gen 1992; 1: 767-788

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