Zellweger SyndromePlasmalogensPeroxisomal DisordersMicrobodiesPeroxisomesSyndromeAdrenoleukodystrophyChondrodysplasia PunctataRefsum DiseaseRefsum Disease, InfantileXylarialesGlyceryl EthersPeroxisomal Multifunctional Protein-2Muscle HypotoniaPipecolic AcidsAcetyl-CoA C-AcetyltransferaseChondrodysplasia Punctata, RhizomelicFibroblastsAcetalsLipid Metabolism, Inborn ErrorsMembrane ProteinsGenetic Complementation TestFatty AcidsPichiaPhosphatidylethanolaminesCatalaseReceptors, Cytoplasmic and NuclearBrain ChemistryMutationCell FusionPhospholipidsDiffuse Cerebral Sclerosis of SchilderCHO CellsBrain InjuriesIntracellular MembranesCricetinaeBrain NeoplasmsCaproatesPelizaeus-Merzbacher DiseaseDown SyndromeMolecular Sequence DataOxidation-ReductionMetabolic Syndrome XAmino Acid Sequence