Bifunctional enzyme deficiency: Identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal β‐oxidation of unknown aetiology by means of complementation analysis

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of inherited metabolic disease 1992-05, Vol.15 (3), p.385-388
Hauptverfasser:	Wanders, R. J. A., Roermund, C. W. T., Brul, S., Schutgens, R. B. H., Tager, J. M.
Format:	Artikel
Sprache:	eng
Schlagworte:	3-Hydroxyacyl CoA Dehydrogenases - deficiency 3-Hydroxyacyl CoA Dehydrogenases - metabolism Acetyl-CoA C-Acetyltransferase - metabolism Acyl-CoA Oxidase Biological and medical sciences Cell Fusion Cells, Cultured Enoyl-CoA Hydratase - deficiency Enoyl-CoA Hydratase - metabolism Errors of metabolism Fibroblasts - enzymology Humans Immunoblotting Infant, Newborn Isomerases - deficiency Isomerases - metabolism Lipids (lysosomal enzyme disorders, storage diseases) Medical sciences Metabolic diseases Metabolism, Inborn Errors - enzymology Microbodies - enzymology Multienzyme Complexes - deficiency Multienzyme Complexes - metabolism Oxidation-Reduction Oxidoreductases - metabolism Peroxisomal Bifunctional Enzyme
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