Neumaier-Probst, E <br/><br/>
Neuroradiological findings in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency).  [electronic resource] 

 -  Journal of inherited metabolic disease  2004 
 - 869-76 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1023/B:BOLI.0000045771.66300.2a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--pathology<br/>Brain--pathology<br/>Glutarates--urine<br/>Glutaryl-CoA Dehydrogenase<br/>Humans<br/>Infant, Newborn<br/>Magnetic Resonance Imaging<br/>Nervous System Diseases--pathology<br/>Oxidoreductases Acting on CH-CH Group Donors--deficiency