They comprise cdg-ia (phosphomannomutase 2 deficiency), cdg-ib (phosphomannose isomerase deficiency), cdg-ic (α-1,3-glucosyltransferase deficiency), cdg-id (α-1,3-mannosyltransferase deficiency), and cdg-ie (dolichol-P-mannose synthase 1 deficiency). cdg-ii are defects in the processing of the N-glycans in the endoplasmic reticulum and the Golgi apparatus and in the synthesis of the O-glycans in the Golgi apparatus.
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