Screening using serum percentage of carbohydrate-deficient transferrin for congenital disorders of glycosylation in children with suspected metabolic disease. [electronic resource]
Producer: 20080212Description: 93-100 p. digitalISSN:- 0009-9147
- Adolescent
- Carbohydrate Metabolism, Inborn Errors -- diagnosis
- Child
- Child, Preschool
- Glycosylation
- Humans
- Infant
- Infant, Newborn
- Isoelectric Focusing
- Mass Screening
- Plasma
- Polymorphism, Genetic
- Protein Isoforms -- blood
- Reference Values
- Serum
- Transferrin -- analogs & derivatives
- alpha 1-Antitrypsin -- blood
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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