A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal β‐oxidation enzyme activities
- 1 May 1990
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (3), 375-379
- https://doi.org/10.1007/bf01799399
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- The inborn errors of peroxisomal β‐oxidation: A reviewJournal of Inherited Metabolic Disease, 1989
- Peroxisomal bifunctional enzyme deficiency.JCI Insight, 1989
- Neonatal seizures and retardation in a girl with biochemical features of X‐linked adrenoleukodystrophyNeurology, 1988
- Bile acid analyses in “pseudo‐Zellweger” syndrome; clues to the defect in peroxisomal β‐oxidationJournal of Inherited Metabolic Disease, 1988