Diagnosis of Congenital Disorders of Glycosylation by Capillary Zone Electrophoresis of Serum Transferrin

Clinical Chemistry

Volumn 50, Issue 1, 2004, Pages 101-111

  Carchon, Hubert A ^a,c   Chevigné, Roland ^b   Falmagne, Jean Bernard ^b   Jaeken, Jaak ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b Analis SA   (Belgium)

^c UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; TRANSFERRIN;

ADOLESCENT; ADULT; ARTICLE; CAPILLARY ZONE ELECTROPHORESIS; CHILD; CONFIDENCE INTERVAL; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; FEMALE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; SCHOOL CHILD; STATISTICAL SIGNIFICANCE; TRANSFERRIN BLOOD LEVEL; TREATMENT OUTCOME;

ADOLESCENT; CARBOHYDRATE METABOLISM, INBORN ERRORS; ELECTROPHORESIS, CAPILLARY; FEMALE; GLYCOSYLATION; HUMANS; ISOELECTRIC FOCUSING; MALE; PROTEIN ISOFORMS; SERUM; TRANSFERRIN;

EID: 1642533464     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2003.021568     Document Type: Article

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