Résumé
Les anomalies congénitales de glycosylation ou CDG (Congenital Disorders of Glycosylation) forment une classe d’erreurs innées du métabolisme, affectant la synthèse des glycannes des glycoprotéines [1, 2]. La glycosylation fait partie des modifications post-traductionnelles et concerne différents types de structures glycannes, la plus connue étant la N-glycosylation.
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Références
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De Lonlay, P., Dubois, S., Valayannopoulos, V., Depondt, E., Ottolenghi, C., Rabier, D. (2013). Défaut de glycosylation des glycoprotéines (CDG). In: Prise en charge médicale et diététique des maladies héréditaires du métabolisme. Springer, Paris. https://doi.org/10.1007/978-2-8178-0046-2_23
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DOI: https://doi.org/10.1007/978-2-8178-0046-2_23
Publisher Name: Springer, Paris
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