Nagan, Narasimhan <br/><br/>
The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C(4)-acylcarnitine concentration in newborn blood spots.  [electronic resource] 

 -  Molecular genetics and metabolism  Apr 2003 
 - 239-46 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1016/s1096-7192(03)00034-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Butyryl-CoA Dehydrogenase--deficiency<br/>Carnitine--analogs & derivatives<br/>Exons<br/>Fatty Acids--metabolism<br/>Gene Frequency<br/>Genetic Variation<br/>Genetics, Population<br/>Genotype<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Mass Screening<br/>Mass Spectrometry<br/>Mutation<br/>Phenotype<br/>Scattering, Radiation<br/>Temperature<br/>United States