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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.
scientific article
Author/s
author: José Antonio Enríquez, Vicente Micol, Patricio Fernández-Silva
Work details
Publication date
June 1, 2000
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Language
English
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