3-hydroxydicarboxylic aciduria—a fatty acid oxidation defect with severe prognosis
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference12 articles.
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2. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes;Roe;J Pediatr,1986
3. Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency;Harpey;J Pediatr,1987
4. Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant death;Bennett;Lancet,1986
5. The inborn error of mitochondrial fatty acid oxidation;Vianey-Liaud;J Inher Metab Dis,1987
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