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Date: 2014-08-13 12:31:27Rare 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 - FINALDisordersDetectableTable42511Add to Reading ListSource URL: www.cdph.ca.govDownload Document from Source WebsiteFile Size: 66,50 KBShare Document on Facebook |
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