Superti-Furga, A <br/><br/>
Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase deficiency): advances and unanswered questions. Report from an international meeting.  [electronic resource] 

 -  European journal of pediatrics  Nov 1997 
 - 821-8 p.  digital 
<br/><br/> Publication Type: Congress; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/s004310050721  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain Diseases--enzymology<br/>Child<br/>Child, Preschool<br/>Developmental Disabilities--enzymology<br/>Female<br/>Glutaryl-CoA Dehydrogenase<br/>Humans<br/>Infant<br/>Metabolism, Inborn Errors--diagnosis<br/>Oxidoreductases--deficiency<br/>Oxidoreductases Acting on CH-CH Group Donors<br/>Pregnancy<br/>Prenatal Diagnosis