Bennett, M J <br/><br/>
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter.  [electronic resource] 

 -  Clinical cardiology  Mar 1996 
 - 243-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Clinical Conference; Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0160-9289 
<br/><br/><label>Standard No.: </label>10.1002/clc.4960190320  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cardiomyopathy, Dilated--etiology<br/>Carnitine--deficiency<br/>Cell Membrane--metabolism<br/>Endocardial Fibroelastosis--etiology<br/>Female<br/>Fibroblasts--metabolism<br/>Genetic Carrier Screening<br/>Homozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Ion Channels--genetics<br/>Ion Transport<br/>Liver--metabolism<br/>Metabolism, Inborn Errors--complications<br/>Muscle, Skeletal--metabolism<br/>Myocardium--metabolism<br/>Skin--metabolism