Peroxisomal DisordersZellweger SyndromeMicrobodiesAdrenoleukodystrophyRefsum DiseasePeroxisomesPhytanic AcidChondrodysplasia Punctata, RhizomelicPlasmalogensChondrodysplasia PunctataPeroxisomal Multifunctional Protein-2Acetyl-CoA C-AcetyltransferaseFatty AcidsLipid Metabolism, Inborn ErrorsAcyl-CoA OxidaseEnoyl-CoA HydratasePeroxisomal Bifunctional EnzymeOxidation-ReductionAcetyl-CoA C-AcyltransferaseGas Chromatography-Mass Spectrometry3-Hydroxyacyl CoA DehydrogenasesFibroblastsGeneticsPichiaBiogenesisClofibrateMolecular Sequence DataCatalaseMembrane ProteinsAmino Acid SequenceReceptors, Cytoplasmic and NuclearCarnitine O-AcetyltransferaseLiverIntracellular MembranesAcyl Coenzyme AMutationBipolar DisorderFungal ProteinsSaccharomyces cerevisiaeBase SequenceProtein TransportSaccharomyces cerevisiae ProteinsOleic AcidOxidoreductasesGlyoxysomesOrganoidsMental DisordersMitochondriaProtein Sorting SignalsAnxiety DisordersMood DisordersClofibric AcidSequence Homology, Amino AcidCarnitine AcyltransferasesCarbon-Carbon Double Bond IsomerasesSubcellular FractionsPhenotypeATP-Binding Cassette TransportersCell FractionationDodecenoyl-CoA IsomeraseGenetics, PopulationPalmitoyl Coenzyme ACloning, MolecularPhytol