Huizing, M <br/><br/>
Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient.  [electronic resource] 

 -  Journal of inherited metabolic disease  Jun 1998 
 - 262-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1023/a:1005324323401  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carnitine--metabolism<br/>Carrier Proteins--genetics<br/>Cells, Cultured<br/>Fatty Acids--metabolism<br/>Female<br/>Fibroblasts<br/>Humans<br/>Infant<br/>Lipid Metabolism, Inborn Errors--genetics<br/>Male