Author Lübke, Torben

1 to 2 of 2 Items
  • 2002 | Journal Article | 
    ​ ​Deficiency of UDP-galactose:N-acetylglucosamine β-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, P. H. et al.​ (2002) 
    Journal of Clinical Investigation, 109 pp. 725​-733​.​ DOI: https://doi.org/10.1172/JCI200214010. 
    ​Details  DOI 
  • 2001 | Journal Article | 
    ​ ​Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency​
    Lübke, T.; Marquardt, T.; Etzioni, A.; Hartmann, E.; Figura, K. von & Körner, C.​ (2001) 
    Nature Genetics, 28 pp. 73​-76​.​ DOI: https://doi.org/10.1038/ng0501-73 
    ​Details  DOI 

Researcher

Göttingen All

Sort

issue date

ASC DESC

Items per Page

10 20 50 100