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]

Kimiko Kasahara, Michinori Funato, Toshiyuki Fukao, Naomi Kondo, Michio Ozeki, Takahide Teramoto, Hideo Kaneko, Shinji Kunishima

doi:10.1016/j.thromres.2010.05.004

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]

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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] Michio Ozeki ⁎, Shinji Kunishima , Kimiko Kasahara , Michinori Funato , Takahide Teramoto , Hideo Kaneko , Toshiyuki Fukao , Naomi Kondo a a Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan b Department of Advanced Diagnosis, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan