Pugliese, Michael <br/><br/>
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review.  [electronic resource] 

 -  Orphanet journal of rare diseases  01 2020 
 - 12 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1750-1172 
<br/><br/><label>Standard No.: </label>10.1186/s13023-019-1276-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Dehydrogenase--deficiency<br/>Humans<br/>Lipid Metabolism, Inborn Errors--enzymology<br/>Phenylketonurias--enzymology<br/>Rare Diseases