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Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007
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acyl CoA dehydrogenase deficiency
enzyme,defect
genetic testing
inborn errors of metabolism
inborn errors of metabolism,screening
mortality
muscular dystrophy,Duchenne,neonatal screening
neonatal screening,genetic neurologic disorders
neurologic disease,diagnoses of
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