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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
Hilbert, Lysiane, Nurden, Paquita, Caron, Claudine, Nurden, Alan, Goudemand, Jenny, Meyer, Dominique, Fressinaud, Edith, Mazurier, ClaudineVolume:
96
Year:
2006
Language:
english
Journal:
Thrombosis and Haemostasis
DOI:
10.1160/TH06-03-0157
File:
PDF, 326 KB
english, 2006