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Tableau I.

Les anomalies congénitales de glycosylation (congenital disorders of glycosylation ou CDG). N-GP : N-glycosylprotéines ; Abs N-GP : absence des chaînes glycaniques des N-GP sériques ; PMM : phosphomannomutase ; PMI : phosphomannose isomérase ; GlcNac : N-acétylglucosamine ; Man : mannose ; Glc : glucose ; MPDU1 : mannose-P-dolichol utilization defect 1.

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