Stevnsner, Tinna <br/><br/>
Mitochondrial repair of 8-oxoguanine is deficient in Cockayne syndrome group B.  [electronic resource] 

 -  Oncogene  Dec 2002 
 - 8675-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0950-9232 
<br/><br/><label>Standard No.: </label>10.1038/sj.onc.1205994  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Cell Line, Transformed<br/>Cockayne Syndrome--genetics<br/>DNA Helicases--genetics<br/>DNA Primers<br/>DNA Repair<br/>DNA Repair Enzymes<br/>DNA, Mitochondrial--genetics<br/>DNA-Formamidopyrimidine Glycosylase<br/>Guanine--analogs & derivatives<br/>Humans<br/>Mice<br/>Mice, Inbred C57BL<br/>N-Glycosyl Hydrolases--metabolism<br/>Poly-ADP-Ribose Binding Proteins