Tansel, Turkan <br/><br/>
A novel ATP8 gene mutation in an infant with tetralogy of Fallot.  [electronic resource] 

 -  Cardiology in the young  Jun 2014 
 - 531-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1467-1107 
<br/><br/><label>Standard No.: </label>10.1017/S1047951113000668  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Phospholipid Transfer Proteins--genetics<br/>Tetralogy of Fallot--genetics