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Date: 2012-08-28 15:52:15Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy | Microsoft Word[removed]Condition list.docAdd to Reading ListSource URL: ndhealth.govDownload Document from Source WebsiteFile Size: 24,51 KBShare Document on Facebook |
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