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Multiple "acyl-CoA" dehydrogenase deficiency
- ... type 2 Glutaric aciduria, type 2 MAD MADD Multiple acyl-CoA dehydrogenase deficiency Multiple FAD dehydrogenase deficiency Genetic Testing Registry: Multiple ...
- ... is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with ... acyl-CoA dehydrogenation deficiency. Hum Mutat. 2003 Jul;22(1):12-23. ...
- ... ETFQO Tests of ETFDH ... ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency. Hum Mutat. 2003 Jul;22(1):12-23. ...
- Genetic Brain Disorders (National Library of Medicine)A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
- ... control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) ... lethal disorder with multiple tissue involvement. J Inherit Metab Dis. 2004;27( ...
- ... and symptoms of isolated long-chain 3-keto-acyl-CoA thiolase deficiency are similar to ... a lethal disorder with multiple tissue involvement. J Inherit Metab Dis. 2004;27( ...