Tein, I <br/><br/>
Fatty acid oxidation abnormalities in childhood-onset spinal muscular atrophy: primary or secondary defect(s)?  [electronic resource] 

 -  Pediatric neurology  Jan 1995 
 - 21-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0887-8994 
<br/><br/><label>Standard No.: </label>10.1016/0887-8994(94)00100-g  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>3-Hydroxyacyl CoA Dehydrogenases--deficiency<br/>Acetyl-CoA C-Acetyltransferase--deficiency<br/>Acetyl-CoA C-Acyltransferase--deficiency<br/>Carnitine--metabolism<br/>Child, Preschool<br/>Fatty Acids--metabolism<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--classification<br/>Male<br/>Mitochondria, Muscle--enzymology<br/>Oxidation-Reduction<br/>Spinal Muscular Atrophies of Childhood--classification