Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide. (Q53601218)
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- Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide. |
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Statements
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide. (English)
Lysiane Hilbert
Paquita Nurden
Claudine Caron
Alan T Nurden
Jenny Goudemand
Dominique Meyer
Edith Fressinaud
Claudine Mazurier
INSERM Network on Molecular Abnormalities in von Willebrand Disease
1 September 2006
96
3
290-294