Villard, J <br/><br/>
Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cells.  [electronic resource] 

 -  Journal of the neurological sciences  Mar 1996 
 - 178-81 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/0022-510x(95)00326-w  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Blotting, Western<br/>Carnitine O-Palmitoyltransferase--deficiency<br/>Cells, Cultured<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Muscle, Skeletal--enzymology<br/>Myoglobinuria--enzymology<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Recurrence