Fig. 1From: Abnormal expression of lysosomal glycoproteins in patients with congenital disorders of glycosylationA diagram showing the location of the defects (the red marks) in the glycosylation pathways in both CDG cases. A The mevalonate pathway and biosynthesis of dolichol on the cytosolic side of the ER and the subsequent glycosylation steps. B UDP-Galactose translocation from the cytoplasm into the GA and its involvement in the galactosyltransferases-mediated galactosylation of glycoconjugatesBack to article page