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
Open Access
- 1 June 2000
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 275 (25), 19198-19209
- https://doi.org/10.1074/jbc.m908734199
Abstract
No abstract availableKeywords
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