Verderio, E <br/><br/>
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations.  [electronic resource] 

 -  Human molecular genetics  Jan 1995 
 - 19-29 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/4.1.19  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Carnitine O-Palmitoyltransferase--deficiency<br/>DNA<br/>DNA Restriction Enzymes--metabolism<br/>Exons<br/>Humans<br/>Introns<br/>Molecular Sequence Data<br/>Mutation<br/>Polymerase Chain Reaction<br/>RNA, Messenger--genetics<br/>Sequence Alignment