Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
Nature Genetics2013Vol. 45(2), pp. 214–219
Citations Over TimeTop 1% of 2013 papers
Cornelia Kornblum, Thomas J. Nicholls, Tobias B. Haack, Susanne Schöler, Viktoriya Peeva, Katharina Danhauser, Kerstin Hallmann, Gábor Zsurka, Joanna Rorbach, Arcangela Iuso, Thomas Wieland, Monica Sciacco, Dario Ronchi, Giacomo P. Comi, Maurizio Moggio, Catarina M. Quinzii, Salvatore DiMauro, Sarah E. Calvo, Vamsi K. Mootha, Thomas Klopstock, Tim M. Strom, Thomas Meitinger, Michal Minczuk, Wolfram S. Kunz, Holger Prokisch
Related Papers
- → Recent developments in the molecular genetics of mitochondrial disorders(1998)80 cited
- → Mitochondrial genome and human mitochondrial diseases(2010)22 cited
- → Heteroplasmy Shifting as Therapy for Mitochondrial Disorders(2019)16 cited
- → Mitochondrial diseases(2002)17 cited
- → Genome editing to treat mitochondrial DNA disorders(2015)