Autosomal dominant type 1 von willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect (Q45867218)
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scientific article published in March 2000
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal dominant type 1 von willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect |
scientific article published in March 2000 |
Statements
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Autosomal dominant type 1 von willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect (English)
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Castaman G
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Missiaglia E
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Rodeghiero F
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1 March 2000
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108
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4
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876-879
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Identifiers
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