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The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.
Glob Med Genet
; 10(4): 278-281, 2023 Dec.
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| MEDLINE | ID: mdl-37822418
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