Identification of pristanoyl‐CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: Implications for Zellweger syndrome

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Veröffentlicht in:Journal of inherited metabolic disease 1991-05, Vol.14 (3), p.349-352
Hauptverfasser: Wanders, R. J. A., Roermund, C. W. T., Jakobs, C., Brink, H. J.
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container_start_page 349
container_title Journal of inherited metabolic disease
container_volume 14
creator Wanders, R. J. A.
Roermund, C. W. T.
Jakobs, C.
Brink, H. J.
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doi_str_mv 10.1007/BF01811700
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Biological and medical sciences
Centrifugation, Density Gradient
Decarboxylation
Errors of metabolism
Humans
Medical sciences
Metabolic diseases
Microbodies - enzymology
Microbodies - metabolism
Miscellaneous hereditary metabolic disorders
Mitochondria, Liver - enzymology
Mitochondria, Liver - metabolism
Oxidoreductases - analysis
Phytanic Acid - metabolism
Zellweger Syndrome - enzymology
Zellweger Syndrome - metabolism
title Identification of pristanoyl‐CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: Implications for Zellweger syndrome
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