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- W1969136838 abstract "The authors regret that an incorrect version of Fig. 3 appeared in the above published article. The correct version appears below. The authors would like to apologize for any inconvenience caused. A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimersThrombosis ResearchVol. 125Issue 2PreviewIn type 2B von Willebrand disease (2B VWD), abnormal von Willebrand factor (VWF) spontaneously binds to platelets. This leads to the clearance of the high molecular weight multimers (HMWM) of VWF and results in thrombocytopenia. Herein we report a family of 2B VWD with an R1306W mutation which caused thrombocytopenia with giant platelets. The most important finding in this study is dynamic changes in VWF values in association with platelet counts. When the proband (2 years of age) had severe thrombocytopenia, his HMWM were normal, however, hematological examination showed a low level of VWF and a lack of HMWM after platelet count recovered. Full-Text PDF" @default.
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- W1969136838 date "2010-10-01" @default.
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- W1969136838 title "Corrigendum to “A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers” [Thrombosis Research 125 (2010) e17–e22]" @default.
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