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.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Zeitschriftentitel
Journal of Clinical Investigation
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109
Zeitschriftennummer
6
Seite
725-733
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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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