Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families (Q37511477)
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scientific article published on 08 June 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families |
scientific article published on 08 June 2009 |
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Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families (English)
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G Castaman
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S Giacomelli
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F Rodeghiero
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8 June 2009
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121
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2-3
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106-110
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