Brassier, Anaïs <br/><br/>
Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome.  [electronic resource] 

 -  Molecular genetics and metabolism  May 2013 
 - 28-32 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1096-7206 
<br/><br/><label>Standard No.: </label>10.1016/j.ymgme.2013.01.017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acidosis, Lactic--blood<br/>Adult<br/>Algeria<br/>Child<br/>Dihydrolipoamide Dehydrogenase--genetics<br/>Female<br/>Humans<br/>Infant<br/>Liver--pathology<br/>Liver Failure, Acute--blood<br/>Male<br/>Maple Syrup Urine Disease--blood<br/>Muscles--pathology<br/>Mutation<br/>Reye Syndrome--genetics