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]

✍ Scribed by Michio Ozeki; Shinji Kunishima; Kimiko Kasahara; Michinori Funato; Takahide Teramoto; Hideo Kaneko; Toshiyuki Fukao; Naomi Kondo

• Book ID: 116914437
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 120 KB
• Volume: 126
• Category: Article
• ISSN: 0049-3848
• DOI: 10.1016/j.thromres.2010.05.004