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Untargeted Metabolomics Identifies Biomarkers for MCADD Neonates in Dried Blood Spots

Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited mitochondrial metabolic disease of fatty acid β-oxidation, especially in newborns. MCADD is clinically diagnosed using Newborn Bloodspot Screening (NBS) and genetic testing. Still, these methods have limitations, suc...

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Detalles Bibliográficos
Autores principales:	Sebaa, Rajaa, AlMogren, Maha, Alseraty, Wafaa, Abdel Rahman, Anas M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253986/ https://www.ncbi.nlm.nih.gov/pubmed/37298607 http://dx.doi.org/10.3390/ijms24119657

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