Zellweger SyndromeSeizuresPeroxisomal DisordersMicrobodiesSyndromePeroxisomesAdrenoleukodystrophyChondrodysplasia PunctataRefsum DiseaseRefsum Disease, InfantilePlasmalogensXylarialesMuscle HypotoniaPeroxisomal Multifunctional Protein-2Pipecolic AcidsAcetyl-CoA C-AcetyltransferaseLipid Metabolism, Inborn ErrorsSeizures, FebrileFibroblastsMembrane ProteinsGenetic Complementation TestPichiaCatalaseEpilepsyMutationCell FusionFatty AcidsAnticonvulsantsDiffuse Cerebral Sclerosis of SchilderReceptors, Cytoplasmic and NuclearIntracellular MembranesAcetalsCHO CellsElectroencephalographyDown SyndromeMetabolic Syndrome XPhenotypeEpilepsies, Partial