Zellweger SyndromeSeizuresPeroxisomal DisordersMicrobodiesSyndromePeroxisomesAdrenoleukodystrophyChondrodysplasia PunctataRefsum DiseaseRefsum Disease, InfantilePlasmalogensXylarialesMuscle HypotoniaPeroxisomal Multifunctional Protein-2Pipecolic AcidsAcetyl-CoA C-AcetyltransferaseLipid Metabolism, Inborn ErrorsSeizures, FebrileVision, OcularFibroblastsVision, LowMembrane ProteinsVision DisordersGenetic Complementation TestPichiaCatalaseEpilepsyMutationVision TestsCell FusionFatty AcidsAnticonvulsantsDiffuse Cerebral Sclerosis of SchilderColor Vision DefectsReceptors, Cytoplasmic and NuclearIntracellular MembranesAcetalsElectroencephalographyCHO CellsDown SyndromeMetabolic Syndrome XPhenotypeVision, BinocularDisease Models, AnimalEpilepsies, Partial