Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference13 articles.
1. Defects in the metabolism of fatty acids in the sudden infant death syndrome;Howatt;BMJ,1985
2. Medium-chain acyl-CoA dehydrogenase deficiency;Stanley,1984
3. Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards;Matsubara;Lancet,1991
4. Screening newborns for multiple organic acidurias in dried filter paper urine samples: method development;Tuchman;Pediatr Res,1991
5. Medium-chain acyl-CoA dehydrogenase deficiency: diagnosis by stable isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine;Rinaldo;N Engl J Med,1998
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