The identification of abnormal glycoforms of serum transferrin in carbohydrate deficient glycoprotein syndrome type I by capillary zone electrophoresis.

Iourin, O; Mattu, T S; Mian, N; Keir, G; Winchester, B; Dwek, R A; Rudd, P M

Iourin, O; Mattu, T S; Mian, N; Keir, G; Winchester, B; Dwek, R A; Rudd, P M.

Affiliation

Iourin O; Department of Biochemistry, University of Oxford, UK.

Glycoconj J ; 13(6): 1031-42, 1996 Dec.

Article in En | MEDLINE | ID: mdl-8981095

Subject(s)

Congenital Disorders of Glycosylation/metabolism; Electrophoresis, Capillary/methods; Transferrin/analysis; Transferrin/chemistry; Carbohydrates/analysis; Carbohydrates/chemistry; Chromatography, High Pressure Liquid; Congenital Disorders of Glycosylation/blood; Congenital Disorders of Glycosylation/diagnosis; Glycoside Hydrolases/metabolism; Humans; N-Acetylneuraminic Acid/analysis; Neuraminidase/metabolism; Polysaccharides/analysis; Polysaccharides/blood; Polysaccharides/chemistry; Sensitivity and Specificity; Transferrin/metabolism; beta-Galactosidase/metabolism

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Collection: 01-internacional Database: MEDLINE Main subject: Transferrin / Electrophoresis, Capillary / Congenital Disorders of Glycosylation Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Glycoconj J Journal subject: BIOQUIMICA / METABOLISMO Year: 1996 Document type: Article Affiliation country: United kingdom

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