A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers

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

• Book ID: 116914218
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 693 KB
• Volume: 125
• Category: Article
• ISSN: 0049-3848
• DOI: 10.1016/j.thromres.2009.08.012