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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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A. Chomyn

Division of Biology

California Institute of Technology

Pasadena

California 91125

USA

[email]@*.bio.caltech.edu

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Division of Biology, California Institute of Technology, Pasadena, California 91125, USA. 2000

References

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes. Chomyn, A., Enriquez, J.A., Micol, V., Fernandez-Silva, P., Attardi, G. J. Biol. Chem. (2000) [Pubmed]

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