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
Zdroj: In Thrombosis Research 2010 125(2):e17-e22
Databáze: ScienceDirect