The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontario

BACKGROUND: Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is a disorder of mitochondrial fatty acid oxidation and is one of the most common inborn errors of metabolism. Identification of MCADD via newborn screening permits the introduction of interventions that can significantly reduce asso...

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Detalles Bibliográficos
Autores principales: Kennedy, Shelley, Potter, Beth K, Wilson, Kumanan, Fisher, Lawrence, Geraghty, Michael, Milburn, Jennifer, Chakraborty, Pranesh
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996355/
https://www.ncbi.nlm.nih.gov/pubmed/21083904
http://dx.doi.org/10.1186/1471-2431-10-82

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996355/
https://www.ncbi.nlm.nih.gov/pubmed/21083904
http://dx.doi.org/10.1186/1471-2431-10-82

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