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