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Rare diseases / Pediatrics / Inborn errors of carbohydrate metabolism / Hepatology / Epidemiology / Newborn screening / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Systemic primary carnitine deficiency / Mitochondrial trifunctional protein deficiency / Health / Medicine / Genetic genealogy
Date: 2011-12-12 15:42:57
Rare diseases
Pediatrics
Inborn errors of carbohydrate metabolism
Hepatology
Epidemiology
Newborn screening
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Systemic primary carnitine deficiency
Mitochondrial trifunctional protein deficiency
Health
Medicine
Genetic genealogy

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