Journal Article Carnitine Gene Mutation Newborn screening S7UI8SM58A 00BH33GNGH Amino Acids Cadmium Citrin deficiency Congenital hypothyroidism DUOX2 protein, human DUOXA2 protein, human Dual Oxidases EC 1.1.1.49 EC 1.11.1.- EC 1.6.3.- EC 1.6.3.1 EC 3.2.1.20 Environmental Pollutants Glucose phosphate dehydrogenase deficiency Glucosephosphate Dehydrogenase LINC00273 lncRNA, human Membrane Glycoproteins Membrane Proteins Mitochondrial Membrane Transport Proteins NADPH Oxidases Newborn screening program Primary carnitine deficiency RNA, Long Noncoding