A family having type 2B von Willebrand disease with an R1306W mutation: Severe thrombocytopenia leads to the normalization of high molecular weight multimers
Autor: | Ozeki, Michio, Kunishima, Shinji, Kasahara, Kimiko, Funato, Michinori, Teramoto, Takahide, Kaneko, Hideo, Fukao, Toshiyuki, Kondo, Naomi |
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Zdroj: | In Thrombosis Research 2010 125(2):e17-e22 |
Databáze: | ScienceDirect |
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