Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: An updated nomenclature for CDG

Glycobiology

Volumn 10, Issue 6, 2000, Pages

  Aebi, M ^a   Helenius, A ^a   Schenk, B ^a   Barone, R ^a   Fiumara, A ^a   Berger, E G ^a   Hennet, T ^a   Imbach, T ^a   Stutz, A ^a   Bjursell, C ^a   Uller, A ^a   Wahlstrom, J G ^a   Briones, P ^a   Cardo, E ^a   Clayton, P ^a   Winchester, B ^a   Cormier Daire, V ^a   De Lonlay, P ^a   Cuer, M ^a   Duprc, T ^a   Seta, N ^a   De Koning, T ^a   Dorland, L ^a   De Loos, F ^a   Kupers, L ^a   Fabritz, L ^a   Hasilik, M ^a   Marquardt, T ^a   Niehues, R ^a   Freeze, H ^a   Grunewald, S ^a   Heykants, L ^a   Jaeken, J ^a   Matthijs, G ^a   Schollen, E ^a   Keir, G ^a   Kjaergaard, S ^a   Schwartz, M ^a   Skovby, F ^a   Klein, A ^a   Roussel, P ^a   Korner, C ^a   Lubke, T ^a   Thiel, C ^a   Von Figura, K ^a   Koscielak, J ^a   Krasnewich, D ^a   Lehle, L ^a   Peters, V ^a   Raab, M ^a   Saether, O ^a   Schachter, H ^a   Van Schaftingen, E ^a   Verbert, A ^a   Vilaseca, A ^a   Wevers, R ^a   Yamashita, K ^a   more..

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

ALG3; ALG6; DPM1; Metabolic disorder; MGAT2; MP1; PMM2

Indexed keywords

CARBOHYDRATE; GLYCOPROTEIN; OLIGOSACCHARIDE; TRANSFERRIN;

CONGENITAL DISORDER OF GLYCOSYLATION; DISEASE CLASSIFICATION; GENE MUTATION; HUMAN; ISOELECTRIC FOCUSING; LETTER; MOLECULAR BIOLOGY; NOMENCLATURE; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; TRANSFERRIN BLOOD LEVEL;

EID: 0034119956     PISSN: 09596658     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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