van Maldegem, B T <br/><br/>
The 625G>A SCAD gene variant is common but not associated with increased C4-carnitine in newborn blood spots.  [electronic resource] 

 -  Journal of inherited metabolic disease  2005 
 - 557-62 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1007/s10545-005-0557-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Butyryl-CoA Dehydrogenase--deficiency<br/>Carnitine--blood<br/>Fatty Acids--metabolism<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--metabolism<br/>Neonatal Screening<br/>Oxygen--metabolism<br/>Polymorphism, Genetic<br/>Polymorphism, Restriction Fragment Length<br/>Time Factors