Tulinius, Már <br/><br/>
Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Jun 2005 
 - 412-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2005.03.010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Biopsy<br/>DNA, Mitochondrial--genetics<br/>Fatal Outcome<br/>Female<br/>Heterozygote<br/>Humans<br/>Infant<br/>Mitochondrial Myopathies--genetics<br/>Molecular Sequence Data<br/>Phenotype<br/>Siblings<br/>Thymidine Kinase--genetics