Date: 2016-03-07 08:48:57Health Medicine Rare diseases Clinical medicine Malonyl-CoA decarboxylase deficiency Glutaric aciduria type 1 Isobutyryl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Inborn error of metabolism Hyperammonemia 2-Methylbutyryl-CoA dehydrogenase deficiency Newborn screening | | IMD Program List of Disorders, Covered Drugs, Supplements and Specialty FoodsAdd to Reading ListSource URL: www.health.gov.on.caDownload Document from Source Website File Size: 298,90 KBShare Document on Facebook
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