Pages that link to "Q72232188"
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The following pages link to Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone (Q72232188):
Displaying 7 items.
- Identification and characterization of new long chain acyl-CoA dehydrogenases (Q24337104) (← links)
- Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation (Q24564364) (← links)
- A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency (Q24676560) (← links)
- Neonatal metabolic myopathies (Q33637042) (← links)
- Medium Chain 3-Ketoacyl-Coenzyme A Thiolase Deficiency: A New Disorder of Mitochondrial Fatty Acid β-Oxidation (Q42546758) (← links)
- Metabolic myopathies (Q71509055) (← links)
- Mitochondrial Disease (Q73701269) (← links)