Author:
Battersby Brendan J.,Loredo-Osti J.C.,Shoubridge Eric A.
Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. DiMauro, S. & Schon, E.A. Mitochondrial DNA mutations in human disease. Am. J. Med. Genet. 106, 18–26 (2001).
2. Larsson, N.G., Holme, E., Kristiansson, B., Oldfors, A. & Tulinius, M. Progressive increase of the mutated mitochondrial DNA fraction in Kearns–Sayre syndrome. Pediatr. Res. 28, 131–136 (1990).
3. Boulet, L., Karpati, G. & Shoubridge, E.A. Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF). Am. J. Hum. Genet. 51, 1187–1200 (1992).
4. Yoneda, M., Chomyn, A., Martinuzzi, A., Hurko, O. & Attardi, G. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Proc. Natl. Acad. Sci. USA 89, 11164–11168 (1992).
5. Kawakami, Y. et al. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes. Ann. Neurol. 35, 370–373 (1994).
Cited by
117 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献