Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation.

Pubmed ID: 
21907147
Year: 
2011
Month: 
SEP
Volume: 
14
Issue: 
3
Citation: 
Tucker EJ., Hershman SG., Köhrer C., Belcher-Timme CA., Patel J., Goldberger OA., Christodoulou J., Silberstein JM., McKenzie M., Ryan MT., Compton AG., Jaffe JD., Carr SA., Calvo SE., RajBhandary UL., Thorburn DR., Mootha VK. Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. Cell Metabolism 14 (3) : 428 - 434(2011) PubMed