Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation I - Callewaert, Nico; Schollen, Els; Vanhecke, Annelies; Jaeken, Jaak; Matthijs, Gert; Contreras, Roland (Glycobiology (Oxford), 2003)
Keywords: 6-pyrenetrisulfonic acid; 8-amino-1; Adult; APTS; asparagine-linked glycosylation; Carbohydrate Metabolism, Inborn Errors - blood; Carbohydrate Metabolism, Inborn Errors - metabolism; CDG; congenital disorder of glycosylation; congenital disorders of glycosylation; DNA sequencer; EDTA; ethylenediaminetetra-acetate; Fucose - chemistry; Fucose - metabolism; glycopathology; Glycoproteins; Glycoproteins - blood; Glycoproteins - chemistry; Glycoproteins - metabolism; Glycoside Hydrolases; Glycosylation; Humans; IEF; Isoelectric Focusing; Liver Cirrhosis - blood; Liver Cirrhosis - metabolism; N-glycan structure; N-glycosylation; Neuraminidase; Oligosaccharides - analysis; phosphomannomutase; Phosphotransferases (Phosphomutases) - deficiency; PMM; Polysaccharides - analysis; Polysaccharides - blood; Sequence Analysis, DNA; Transferrin - analysis; Transferrin - metabolism