A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal β‐oxidation enzyme activities

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Veröffentlicht in:	Journal of inherited metabolic disease 1990, Vol.13 (3), p.375-379
Hauptverfasser:	Wanders, R. J. A., Roermund, C. W. T., Schelen, A., Schutgens, R. B. H., Tager, J. M., Stephenson, J. B. P., Clayton, P. T.
Format:	Artikel
Sprache:	eng
Schlagworte:	3-Hydroxyacyl CoA Dehydrogenases - deficiency Acatalasia Aminoacid disorders Biological and medical sciences Cell Fractionation Cells, Cultured Enoyl-CoA Hydratase - deficiency Errors of metabolism Fibroblasts - ultrastructure Humans Isomerases Medical sciences Metabolic diseases Microbodies - enzymology Multienzyme Complexes - deficiency Oxidation-Reduction Peroxisomal Bifunctional Enzyme Zellweger Syndrome - enzymology
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