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Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG)

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Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups

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The underglycosylation of plasma α 1 -antitrypsin in congenital disorders of glycosylation type I is not random

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