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Rare diseases / Newborn screening / Carnitine-acylcarnitine translocase deficiency / Fatty-acid metabolism disorder / Carnitine / Phenylketonuria / Glutaric aciduria type 1 / Systemic primary carnitine deficiency / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Health / Medicine / Genetic genealogy
Date: 2014-08-13 12:31:27
Rare diseases
Newborn screening
Carnitine-acylcarnitine translocase deficiency
Fatty-acid metabolism disorder
Carnitine
Phenylketonuria
Glutaric aciduria type 1
Systemic primary carnitine deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Health
Medicine
Genetic genealogy

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