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Date: 2013-07-08 12:47:26Genetic genealogy Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Propionic acidemia Malonyl-CoA decarboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Medicine | Newborn Screening Program DisordersAdd to Reading ListSource URL: health.utah.govDownload Document from Source WebsiteFile Size: 56,50 KBShare Document on Facebook |
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