Genetic heterogeneity in patients with a disorder of peroxisomal β-oxidation: A complementation study based on pristanic acid β-oxidation suggesting different enzyme defects

Journal of Inherited Metabolic Disease

Volumn 20, Issue 3, 1997, Pages 437-440

  Van Grunsven, E G ^a   Wanders, R J A ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYL COENZYME A ACETYLTRANSFERASE; ACYL COENZYME A OXIDASE; BILE ACID; CHENODEOXYCHOLIC ACID; CHOLIC ACID; ENZYME; FATTY ACID; PRISTANIC ACID; STEROL CARRIER PROTEIN; UNCLASSIFIED DRUG;

ADRENOLEUKODYSTROPHY; BILE ACID SYNTHESIS; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME ACTIVITY; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FIBROBLAST CULTURE; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; MITOCHONDRION; PEROXISOME; SKIN FIBROBLAST;

FATTY ACIDS; FIBROBLASTS; GENETIC COMPLEMENTATION TEST; HUMANS; OXIDATION-REDUCTION; PEROXISOMAL DISORDERS; SKIN;

EID: 0030798966     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005323221660     Document Type: Conference Paper

References (14)

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