A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients
- 1 December 1992
- journal article
- case report
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 1 (9) , 767-768
- https://doi.org/10.1093/hmg/1.9.767
Abstract
Z.P. Zhang, G. Falk, M. Blombäck, N. Egberg, M. Anveret; A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation inKeywords
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