Tavasoli, Ali Reza <br/><br/>
Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review.  [electronic resource] 

 -  Brain & development  Sep 2017 
 - 714-716 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1872-7131 
<br/><br/><label>Standard No.: </label>10.1016/j.braindev.2017.04.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--diagnostic imaging<br/>Child, Preschool<br/>Developmental Disabilities--diagnostic imaging<br/>Enoyl-CoA Hydratase--genetics<br/>Humans<br/>Male<br/>Metabolism, Inborn Errors--diagnostic imaging<br/>Mutation<br/>RNA-Binding Proteins--genetics