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.
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| Description | scientific article |
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author: Vicente Micol José Antonio Enríquez Patricio Fernández-Silva |
| Publication date | June 1, 2000 |
| Language | English |
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