Bifunctional protein deficiency: Complementation within the same group suggesting differential enzyme defects and clues to the underlying basis

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Bibliographic Details
Published in:Journal of inherited metabolic disease 1998-06, Vol.21 (3), p.298-301
Main Authors: Grunsven, E. G., Berkel, E., Lemonde, H., Clayton, P. T., Wanders, R. J. A.
Format: Article
Language:English
Subjects:
3-Hydroxyacyl CoA Dehydrogenases - metabolism
Biological and medical sciences
Cells, Cultured
Enoyl-CoA Hydratase - metabolism
Errors of metabolism
Humans
Isomerases
Lipids (lysosomal enzyme disorders, storage diseases)
Medical sciences
Metabolic diseases
Multienzyme Complexes - metabolism
Peroxisomal Bifunctional Enzyme
Peroxisomal Disorders - enzymology
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ISSN:0141-8955
1573-2665
DOI:10.1023/A:1005396912015