Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId

Hansske B, Thiel C, Lübke T, Hasilik M, Höning S, Peters V, Heidemann PH, Hoffmann GF, Berger EG, von Figura K, Körner C (2002)
Journal of Clinical Investigation 109(6): 725-733.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Hansske, Bengt; Thiel, Christian; Lübke, TorbenUniBi; Hasilik, Martin; Höning, Stefan; Peters, Verena; Heidemann, Peter H.; Hoffmann, Georg F.; Berger, Eric G.; von Figura, Kurt; Körner, Christian
Erscheinungsjahr
2002
Zeitschriftentitel
Journal of Clinical Investigation
Band
109
Ausgabe
6
Seite(n)
725-733
Page URI
https://pub.uni-bielefeld.de/record/1940103

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Hansske B, Thiel C, Lübke T, et al. Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. Journal of Clinical Investigation. 2002;109(6):725-733.
Hansske, B., Thiel, C., Lübke, T., Hasilik, M., Höning, S., Peters, V., Heidemann, P. H., et al. (2002). Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. Journal of Clinical Investigation, 109(6), 725-733.
Hansske, B., Thiel, C., Lübke, T., Hasilik, M., Höning, S., Peters, V., Heidemann, P. H., Hoffmann, G. F., Berger, E. G., von Figura, K., et al. (2002). Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. Journal of Clinical Investigation 109, 725-733.
Hansske, B., et al., 2002. Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. Journal of Clinical Investigation, 109(6), p 725-733.
B. Hansske, et al., “Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId”, Journal of Clinical Investigation, vol. 109, 2002, pp. 725-733.
Hansske, B., Thiel, C., Lübke, T., Hasilik, M., Höning, S., Peters, V., Heidemann, P.H., Hoffmann, G.F., Berger, E.G., von Figura, K., Körner, C.: Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId. Journal of Clinical Investigation. 109, 725-733 (2002).
Hansske, Bengt, Thiel, Christian, Lübke, Torben, Hasilik, Martin, Höning, Stefan, Peters, Verena, Heidemann, Peter H., Hoffmann, Georg F., Berger, Eric G., von Figura, Kurt, and Körner, Christian. “Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId”. Journal of Clinical Investigation 109.6 (2002): 725-733.

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