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Items for "Type 1VWD,VWF gene mutations"

An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease

Forty families diagnosed by UK centres to have type 1 VWD were recruited. Following review, six families were re-diagnosed to have type 2 VWD, one to have a platelet storage pool disorder, and one family was determined to be unaffected...

Keywords: Type 1VWD,VWF gene mutations, inherited bleeding disorders, molecular pathogenesis

11/2006 | Thrombosis and Haemostasis, Schattauer