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7
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"Acyl-CoA" dehydrogenase "family," member "9," deficiency of
- ... condition. Acyl-CoA dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 Mitochondrial complex I deficiency due to ACAD9 deficiency Genetic Testing Registry: Acyl- ...
- ... MedlinePlus Genetics provides information about Mitochondrial complex I deficiency More About This Health Condition acyl-CoA dehydrogenase family member 9, mitochondrial acyl-Coenzyme A dehydrogenase family, member 9 ...
- ... AW, Wendel U. MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency. J Pediatr. 2003 Sep;143(3):335-42. ...
- ... AW, Wendel U. MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency. J Pediatr. 2003 Sep;143(3):335-42. ...
- ... J. Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center's experience. Genet Med. 2012 Mar;14(3):342-7. doi: 10.1038/gim.2011.9. Epub 2012 Jan 5. Citation on PubMed van ...
- ... reduced energy production and the features of IBD deficiency. More About This Health Condition ACAD-8 ACAD8_HUMAN Activator-recruited cofactor 42 kDa component acyl-CoA dehydrogenase family, member 8 acyl-coenzyme A dehydrogenase 8 ARC42 ...
- ... mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. Mol ... deficiency: clinical, biochemical, and pathological studies on three subjects ...