Peroxisomal DisordersZellweger SyndromePeroxisomesMicrobodiesRefsum Disease, InfantileRefsum DiseaseAdrenoleukodystrophyChondrodysplasia Punctata, RhizomelicMembrane ProteinsGenetic Complementation TestReceptors, Cytoplasmic and NuclearFibroblastsAdenosine TriphosphatasesMutationBiogenesisAcyl-CoA OxidaseEnoyl-CoA HydratasePeroxisomal Bifunctional EnzymePeroxisomal Multifunctional Protein-2Acetyl-CoA C-AcetyltransferaseAcetyl-CoA C-AcyltransferaseBipolar Disorder3-Hydroxyacyl CoA DehydrogenasesPichiaMental DisordersMolecular Sequence DataClofibrateAnxiety DisordersMood DisordersAmino Acid SequenceCatalaseFatty AcidsPhytanic AcidIntracellular MembranesMitochondrial TurnoverSaccharomyces cerevisiaeLiverSaccharomyces cerevisiae ProteinsProtein TransportCarnitine O-AcetyltransferaseMitochondriaOxidation-ReductionDiagnostic and Statistical Manual of Mental DisordersAcyl Coenzyme AFungal ProteinsBase SequenceOleic AcidOxidoreductasesDepressive Disorder, MajorOrganoidsGlyoxysomesPlasmalogensAttention Deficit Disorder with HyperactivityProtein Sorting SignalsSequence Homology, Amino AcidMitochondrial ProteinsDepressive DisorderSubcellular FractionsATP-Binding Cassette Transporters