A Deficiency in Dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl α3-Glucosyltransferase Defines a New Subtype of Congenital Disorders of Glycosylation*
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P. Codogno | O. Danos | R. Oriol | T. Dupré | I. Chantret | G. Durand | Julia Dancourt | S. Vuillaumier‐Barrot | N. Seta | H. Ogier de Baulny | C. Delenda | S. Moore | Stéphanie Bucher | Celine Peletan | T. Dupré