Baruteau, Julien <br/><br/>
Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.  [electronic resource] 

 -  Journal of inherited metabolic disease  Sep 2013 
 - 795-803 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study 
<br/><br/><label>ISSN: </label>1573-2665 
<br/><br/><label>Standard No.: </label>10.1007/s10545-012-9542-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Dehydrogenase--deficiency<br/>Acyl-CoA Dehydrogenase, Long-Chain--deficiency<br/>Child<br/>Child, Preschool<br/>Fatty Acids--metabolism<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--diagnosis<br/>Male<br/>Mitochondria--metabolism<br/>Oxidation-Reduction<br/>Retrospective Studies