Dimmock, D P <br/><br/>
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.  [electronic resource] 

 -  Human mutation  Feb 2008 
 - 330-1 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.9519  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child, Preschool<br/>DNA, Mitochondrial--genetics<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation--genetics<br/>Organ Specificity<br/>Phosphotransferases (Alcohol Group Acceptor)--genetics