PeroxisomesEnoyl-CoA HydrataseFatty AcidsOxidation-ReductionMicrobodiesPeroxisomal DisordersLipid MetabolismPoint MutationLiverMutation, MissenseMutationAcyl-CoA OxidasePeroxisomal Bifunctional EnzymeZellweger SyndromePeroxisomal Multifunctional Protein-2Frameshift MutationMolecular Sequence DataAcetyl-CoA C-AcyltransferaseAcetyl-CoA C-AcetyltransferaseBase SequenceAdrenoleukodystrophy3-Hydroxyacyl CoA DehydrogenasesAmino Acid SequenceGerm-Line MutationClofibrateInterleukin-1betaMembrane ProteinsPichiaCatalasePedigreeKineticsOxidoreductasesReceptors, Cytoplasmic and NuclearPhytanic AcidSequence Homology, Amino AcidCloning, MolecularCarnitine O-AcetyltransferaseExonsAmino Acid Substitutionbeta 2-MicroglobulinMutation RatePolymerase Chain ReactionCell LineMutagenesis, Site-DirectedSaccharomyces cerevisiaeFungal ProteinsDNA PrimersRefsum DiseaseBinding SitesHeterozygoteIntracellular MembranesMutagenesisDNA Mutational AnalysisAcyl Coenzyme ARNA, MessengerModels, MolecularAllelesCells, CulturedOleic AcidRecombinant ProteinsSequence AlignmentEscherichia coliSaccharomyces cerevisiae ProteinsSequence Analysis, DNAProtein TransportGenetic Complementation TestPhenotypeGenotypeIntegrin beta3Receptors, Adrenergic, betaOrganoidsHomozygoteMitochondria, LiverCarrier ProteinsTransfectionProtein Structure, TertiaryGlyoxysomesPolymorphism, Single-Stranded ConformationalTranscription FactorsRecombinant Fusion ProteinsMitochondriaProtein BindingHydrogen PeroxideGene DeletionPlasmalogensSequence DeletionSignal TransductionDNACarnitine AcyltransferasesProtein Sorting SignalsPalmitoyl Coenzyme ASubcellular FractionsFibroblastsCarbon-Carbon Double Bond IsomerasesCodon, NonsenseClofibric AcidATP-Binding Cassette TransportersMethanolAlcohol OxidoreductasesPlasmids