A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients (Q48146952)
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scientific article published on December 1, 1992
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients |
scientific article published on December 1, 1992 |
Statements
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A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients (English)
Z. P. Zhang
G. Falk
M. Blombäck
N. Egberg
1 December 1992
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1
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9
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767-768
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Identifiers
1 reference