Corydon, M J <br/><br/>
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.  [electronic resource] 

 -  Pediatric research  Jan 2001 
 - 18-23 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0031-3998 
<br/><br/><label>Standard No.: </label>10.1203/00006450-200101000-00008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Dehydrogenase<br/>Acyl-CoA Dehydrogenases--genetics<br/>DNA, Complementary<br/>Female<br/>Genetic Variation<br/>Haplotypes<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--genetics<br/>Male<br/>Mutagenesis, Site-Directed<br/>Mutation