van Maldegem, B T <br/><br/>
High prevalence of short-chain acyl-CoA dehydrogenase deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood.  [electronic resource] 

 -  Neuropediatrics  Feb 2011 
 - 13-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1439-1899 
<br/><br/><label>Standard No.: </label>10.1055/s-0031-1275342  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Dehydrogenase--deficiency<br/>Adolescent<br/>Butyryl-CoA Dehydrogenase--genetics<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Epilepsy--epidemiology<br/>Female<br/>Humans<br/>Incidence<br/>Infant<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--diagnosis<br/>Male<br/>Mutation--genetics<br/>Netherlands--epidemiology<br/>Pediatrics