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Angeborene Störungen der Glykosylierung (CDG-Syndrome)

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Pädiatrie
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Zusammenfassung

„Congenital disorders of glycosylation“ sind angeborene Erkrankungen, hervorgerufen durch inkorrekte Glykosylierung von Proteinen. Die Erkrankungen wurden bisher als „Carbohydrate-deficient“ Glykoproteinsyndrome (CDG-S) bezeichnet.

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Literatur

  • Jaeken J, Matthijs G, Carchon H, von Schaftingen E (2001) Defects of N-glycan synthesis. In: Scriver Ch R, Beaudet AL, Sly WS, Valle D (eds). The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 1601–1622

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© 2003 Springer-Verlag Berlin Heidelberg

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Ullrich, K., Harms, E. (2003). Angeborene Störungen der Glykosylierung (CDG-Syndrome). In: Lentze, M.J., Schulte, F.J., Schaub, J., Spranger, J. (eds) Pädiatrie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-09176-0_35

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  • DOI: https://doi.org/10.1007/978-3-662-09176-0_35

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-09177-7

  • Online ISBN: 978-3-662-09176-0

  • eBook Packages: Springer Book Archive

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