A tRNA suppressor mutation in human mitochondria
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0498-350.pdf
Reference25 articles.
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3. Dunbar, D.R., Moonie, P.A., Jacobs, H.T. & Holt, I.J. Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes. Proc. Natl. Acad. Sci. USA 92, 6562–6566 (1995).
4. Dunbar, D.R., Moonie, P.A., Zeviani, M. & Holt, I.J. Complex I deficiency is associated with 3243G/C mitochondrial DNA in osteosarcoma cell cybrids. Hum. Mol. Genet. 5, 123–129 (1996).
5. King, M.P., Koga, Y., Davidson, M. & Schon, E.A. Defects in mitochondrial protein-synthesis and respiratory-chain activity segregate with the transfer RNA(leu)(UUR) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Mol. Cell. Biol. 12, 480–490 (1992).
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