Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: Unequivocal evidence for differential defects in the same enzyme protein

Biochemical and Biophysical Research Communications

Volumn 235, Issue 1, 1997, Pages 176-179

  Van Grunsven, E G ^a   Van Roermund, C W T ^a   Denis, S ^a   Wanders, R J A ^a  

^a EMMA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ENOYL COENZYME A HYDRATASE; FATTY ACID;

ARTICLE; CELL FUSION; CLINICAL ARTICLE; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FIBROBLAST; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; METABOLIC DISORDER; PEROXISOME; PRIORITY JOURNAL; SOMATIC CELL;

EID: 0031560948     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1997.6755     Document Type: Article

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