其他A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.
期刊:Thrombosis and haemostasis发表年份:2005作者:Gergely Losonczy; Nurit Rosenberg; Csongor Kiss; János Kappelmayer; György Vereb; Adrienne Kerényi; István Balogh; László Muszbek
