Zellweger SyndromePeroxisomal DisordersMicrobodiesSyndromePeroxisomesAdrenoleukodystrophyChondrodysplasia PunctataRefsum DiseaseRefsum Disease, InfantilePlasmalogensXylarialesPeroxisomal Multifunctional Protein-2Muscle HypotoniaPipecolic AcidsAcetyl-CoA C-AcetyltransferaseLipid Metabolism, Inborn ErrorsFibroblastsMembrane ProteinsGenetic Complementation TestPichiaCatalaseCell FusionFatty AcidsMutationReceptors, Cytoplasmic and NuclearDiffuse Cerebral Sclerosis of SchilderIntracellular MembranesAcetalsCHO CellsDown SyndromeMetabolic Syndrome X