Hypoglycosylation of a brain glycoprotein (β-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl- transferase II deficiency

Glycobiology

Volumn 7, Issue 8, 1997, Pages 1077-1084

  Pohl, Susanne ^b   Hoffmann, Andrea ^b   Rüdiger, Angelika ^a   Nimtz, Manfred ^a   Jaeken, Jaak ^a   Conradt, Harald S ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

Author keywords

'Brain type' N glycosylation; Carbohydrate deficiency glycoprotein syndrome; GlcNAc transferase II deficiency; Human trace protein; Human cerebrospinal fluid; Phosphomannomutase deficiency

Indexed keywords

MUTASE; N ACETYLGLUCOSAMINYLTRANSFERASE;

ARTICLE; CARBOHYDRATE ANALYSIS; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; ENZYME DEFICIENCY; HUMAN; IMMUNOBLOTTING; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN GLYCOSYLATION;

ADULT; BETA-GLOBULINS; BLOTTING, WESTERN; BRAIN; CARBOHYDRATE CONFORMATION; CARBOHYDRATE SEQUENCE; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; ELECTROPHORESIS, POLYACRYLAMIDE GEL; GLYCOSYLATION; HUMANS; INTRAMOLECULAR OXIDOREDUCTASES; MASS SPECTROMETRY; METHYLATION; MOLECULAR SEQUENCE DATA; N-ACETYLGLUCOSAMINYLTRANSFERASES; OLIGOSACCHARIDES; PHOSPHOTRANSFERASES (PHOSPHOMUTASES);

EID: 0031472368     PISSN: 09596658     EISSN: None     Source Type: Journal    
DOI: 10.1093/glycob/7.8.1077     Document Type: Article

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