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Date: 2009-02-03 16:52:18Medical genetics Newborn screening Organic acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)Add to Reading ListSource URL: www.health.mo.govDownload Document from Source WebsiteFile Size: 18,33 KBShare Document on Facebook |