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Rare diseases / Medium-chain acyl-coenzyme A dehydrogenase deficiency / Newborn screening / Very long-chain acyl-coenzyme A dehydrogenase deficiency / Fatty-acid metabolism disorder / Acyl CoA dehydrogenase / Phenylketonuria / Mitochondrial trifunctional protein / Inborn error of lipid metabolism / Health / Genetic genealogy / Medical genetics


MS/MS-BASED NEWBORN AND FAMILY SCREENING DETECTS ASYMPTOMATIC PATIENTS WITH VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY UTE SPIEKERKOETTER, MD, BIN SUN, MD, THOMAS ZYTKOVICZ, PHD, RONALD WANDERS, PHD, ARNOLD W. STR
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Document Date: 2012-05-31 13:41:14


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