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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


Microsoft Word - FINALDisordersDetectableTable42511
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Document Date: 2014-08-13 12:31:27

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File Size: 66,50 KB

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