High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
Nature Genetics2010Vol. 42(10), pp. 851–858
Citations Over TimeTop 1% of 2010 papers
Sarah E. Calvo, Elena J. Tucker, Alison G. Compton, Denise M. Kirby, Gabriel Crawford, Noël P. Burtt, Manuel A. Rivas, Candace Guiducci, Damien L. Bruno, Olga Goldberger, Michelle C Redman, Esko Wiltshire, Callum Wilson, David Altshuler, Stacey B. Gabriel, Mark J. Daly, David R. Thorburn, Vamsi K. Mootha
Related Papers
- → DUPLICATIONS OF MITOCHONDRIAL DNA IN MITOCHONDRIAL MYOPATHY(1989)203 cited
- → Depletion of mitochondrial DNA in the skeletal muscle of two cirrhotic patients with severe asthenia(2002)13 cited
- → Maternal transmission of mitochondrial DNA in ducks(1990)9 cited
- 印度人群线粒体 DNA 系统发育基因组学研究(2006)
- → Μελέτη της ετεροπλασμίας του μιτοχονδριακού DNA σε εργαστηριακά στελέχη Drosophila και σε φυσικούς υβριδικούς πληθυσμούς(2022)