Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: primary or secondary defect(s)? [electronic resource]
Producer: 19950621Description: 21-30 p. digitalISSN:- 0887-8994
- 3-Hydroxyacyl CoA Dehydrogenases -- deficiency
- Acetyl-CoA C-Acetyltransferase -- deficiency
- Acetyl-CoA C-Acyltransferase -- deficiency
- Carnitine -- metabolism
- Child, Preschool
- Fatty Acids -- metabolism
- Female
- Humans
- Infant
- Infant, Newborn
- Lipid Metabolism, Inborn Errors -- classification
- Male
- Mitochondria, Muscle -- enzymology
- Oxidation-Reduction
- Spinal Muscular Atrophies of Childhood -- classification
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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