其他Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.
期刊:Blood发表年份:2005作者:Ivan Martinez-Duncker; Thierry Dupré; Véronique Piller; Friedrich Piller; Jean-Jacques Candelier; Catherine Trichet; Gil Tchernia; Rafael Oriol; Rosella Mollicone
