Peroxisomal DisordersZellweger SyndromeRefsum DiseaseAdrenoleukodystrophyMicrobodiesChondrodysplasia Punctata, RhizomelicPhytanic AcidPlasmalogensPeroxisomesChondrodysplasia PunctataFatty AcidsPeroxisomal Multifunctional Protein-2Acetyl-CoA C-AcetyltransferaseLipid Metabolism, Inborn ErrorsAcyl-CoA OxidasePeroxisome ProliferatorsOxidation-ReductionGas Chromatography-Mass SpectrometryFibroblastsGeneticsReceptors, Cytoplasmic and NuclearPPAR gammaEnoyl-CoA HydrataseBiogenesisPeroxisomal Bifunctional EnzymeClofibratePeroxisome Proliferator-Activated ReceptorsAcetyl-CoA C-AcyltransferasePPAR alpha3-Hydroxyacyl CoA DehydrogenasesMolecular Sequence DataPichiaBipolar DisorderThiazolidinedionesMembrane ProteinsClofibric AcidLiverTranscription FactorsMutationAmino Acid SequenceMental DisordersCatalaseFibric AcidsAnxiety DisordersMood DisordersBase SequenceIntracellular MembranesSaccharomyces cerevisiaeMitochondrial TurnoverSaccharomyces cerevisiae ProteinsMitochondriaGenetics, PopulationProtein TransportPPAR deltaCarnitine O-AcetyltransferaseFungal Proteins