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2000
Mark Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation : An updated nomenclature for CDG
Aebi, M. ; Helenius, A. ; Schenk, B. ; Barone, R. ; Fiumara, A. ; Berger, E. G. ; Hennet, T. ; Imbach, T. ; Stutz, A. ^LU and Bjursell, C. , et al. (2000) In Glycobiology 16. p.669-671
- Contribution to journal › Letter
1999
Mark Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation : An updated nomenclature for CDG
Aebi, M. ; Helenius, A. ; Schenk, B. ; Barone, R. ; Fiumara, A. ; Berger, E. G. ; Hennet, T. ; Imbach, T. ; Stutz, A. and Bjursell, C. , et al. (1999) In Glycoconjugate Journal 16(11). p.669-671
- Contribution to journal › Letter
1997
Mark Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins
Jaeken, J. ; Artigas, J. ; Barone, R. ; Fiumara, A. ; De Koning, T. J. ^LU ; Poll-The, B. T. ; De Rijk-Van Andel, J. F. ; Hoffmann, G. F. ^LU ; Assmann, B. and Mayatepek, E. , et al. (1997) In Journal of Inherited Metabolic Disease 20(3). p.447-449
- Contribution to journal › Article