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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Библиографические подробности
Главные авторы: Kennedy, Shelley, Potter, Beth K, Wilson, Kumanan, Fisher, Lawrence, Geraghty, Michael, Milburn, Jennifer, Chakraborty, Pranesh
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2010
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2996355/
https://ncbi.nlm.nih.gov/pubmed/21083904
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-10-82
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