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

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Bibliographic Details
Published in:	Journal of inherited metabolic disease 1997-07, Vol.20 (3), p.437-440
Main Authors:	Grunsven, E. G., Wanders, R. J. A.
Format:	Article
Language:	English
Subjects:	Biological and medical sciences Errors of metabolism Fatty Acids - metabolism Fibroblasts - enzymology Fibroblasts - metabolism Genetic Complementation Test Humans Lipids (lysosomal enzyme disorders, storage diseases) Medical sciences Metabolic diseases Oxidation-Reduction Peroxisomal Disorders - enzymology Peroxisomal Disorders - genetics Peroxisomal Disorders - metabolism Skin - enzymology Skin - metabolism
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