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...

Descripción completa

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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253986/
https://www.ncbi.nlm.nih.gov/pubmed/37298607
http://dx.doi.org/10.3390/ijms24119657

Ejemplares similares