Biosynthesis of peroxisomal β-oxidation enzymes in infants with zellweger syndrome
- 1 September 1986
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 9 (3) , 292-296
- https://doi.org/10.1007/bf01799668
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Peroxisomal β-oxidation enzyme proteins in the Zellweger syndromeBiochemical and Biophysical Research Communications, 1985
- Peroxisomal Defects in Neonatal-Onset and X-Linked AdrenoleukodystrophiesScience, 1985
- Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)Nature, 1983
- Purification and Properties of Carnitine Octanoyltransferase and Carnitine Palmitoyltransferase from Rat Liver1The Journal of Biochemistry, 1983
- Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids.1982
- Properties of Mitochondrial and Peroxisomal Enoyl-CoA Hydratases from Rat Liver1The Journal of Biochemistry, 1980
- The Presence of a New 3‐Oxoacyl‐CoA Thiolase in Rat Liver PeroxisomesEuropean Journal of Biochemistry, 1980
- Cell-free synthesis and processing of a putative precursor for mitochondrial carbamyl phosphate synthetase I of rat liverProceedings of the National Academy of Sciences, 1979
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973