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Date: 2011-12-12 15:42:57Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy | Microsoft Word - pocket facts.docxAdd to Reading ListSource URL: ndhealth.govDownload Document from Source WebsiteFile Size: 51,98 KBShare Document on Facebook |