Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability
Direnis Erdinc(University of Gothenburg), Thomas J. Nicholls(Wellcome Centre for Mitochondrial Research)
Cited by 28
Related Papers
Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
|The American Journal of Human Genetics|2014|157