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Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency

Significant Clinical HeterogeneityMendelian DisorderAutoimmune DiseaseSimilar Etfdh GenotypeGenetic DisorderGeneticsInherited Metabolic DiseaseMetabolic DiseaseGenetic EpidemiologyPathologyHuman PolymorphismDisease Gene IdentificationMedicineAtherosclerosisChinese Patients