Congenital Disorders of GlycosylationGlycosylationCarbohydrate Metabolism, Inborn ErrorsPhosphotransferases (Phosphomutases)MannosyltransferasesMannose-6-Phosphate IsomeraseMuscle HypertoniaPolysaccharidesDolicholProtein Modification, TranslationalTransferrinMetabolism, Inborn ErrorsHirschsprung DiseaseMutationOligosaccharidesFucoseIsoelectric FocusingAbnormalities, MultipleMolecular Sequence DataMannoseLeukocyte-Adhesion Deficiency SyndromeExomeGolgi ApparatusGlycoproteinsAmino Acid SequenceCarbohydrate SequenceSyndromeBipolar DisorderTunicamycinGlucosyltransferasesFibroblastsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationCaroli DiseaseAdaptor Proteins, Vesicular TransportPhenotypeCongenital AbnormalitiesGenetic Diseases, InbornMental DisordersInfant, NewbornFatal OutcomeEndoplasmic ReticulumAnxiety DisordersDNA Mutational AnalysisGenes, RecessiveMembrane ProteinsMood DisordersPedigreeBase SequenceCHO CellsMutation, MissenseIntellectual DisabilityAsparagineHomozygoteProtein Processing, Post-TranslationalDiagnostic and Statistical Manual of Mental DisordersChromatography, High Pressure LiquidPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseProtein IsoformsCells, CulturedGlycopeptidesDepressive Disorder, MajorGlycosyltransferasesAttention Deficit Disorder with HyperactivityDisease Models, AnimalDepressive DisorderSequence Analysis, DNACarbohydrate ConformationGlycomicsN-AcetylglucosaminyltransferasesObsessive-Compulsive Disorder