Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference50 articles.
1. A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
2. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
3. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
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