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Thromb Haemost 1993; 70(06): 1064-1065
DOI: 10.1055/s-0038-1649727
DOI: 10.1055/s-0038-1649727
Letter to the Editor
ΔC in Exon 18 of the von Willebrand Gene Is Uncommon in German vWD Type III Patients
Further Information
Publication History
Received 11 June 1993
Accepted after revision 19 August 1993
Publication Date:
26 July 2018 (online)
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References
- 1 Ruggeri ZM, Zimmermann TS. von Willebrand factor and von Willebrand disease. Blood 1987; 70: 895-904
- 2 Mancuso DJ, Tuley EA, Westfield LA, Worrall NK, Shelton-Inloes BB, Sorace JM, Alevy YG, Sadler JE. Structure of the gene for human von Willebrand factor. J Biol Chem 1989; 264: 19514-19527
- 3 Ginsburg D, Sadler JE. Von Willebrand disease: A database of point mutations insertions, and deletions. Thromb Haemostas 1993; 69: 177-184
- 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
- 5 Faber JP, Poller W, Olek K, Baumann U, Carlson J, Lindmark B, Eriksson S. The molecular basis of α1-antichymotrypsin deficiency in a heterozygote with liver and lung disease. J Hepatol. 1993 (in press)
- 6 Mertes G, Ludwig M, Schwaab R, Brackmann H-H, Olek K. T/C polymorphism in the von Willebrand factor (vWF) gene at codon 795. Hum Mol Gen. 1993. (submitted)