ArticleGlobal medical genetics2023

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.

Maha Alotaibi et al.PubMed ↗Full text ↗Publisher ↗

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