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Combination of postmortem mass spectrometry imaging and genetic analysis reveals very long-chain acyl-CoA dehydrogenase deficiency in a case of infant death with liver steatosis

Genetic Analysis RevealsHepatologyBiochemistryLiver PhysiologyInherited Metabolic DiseaseLiver SteatosisPathologyLiver DiseaseFatty Liver DiseaseMetabolismMedicineInfant Death