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Human Molecular Genetics, Vol. 10, Iss. 6, 2001-03 ,pp. : 573-580

Oxford University Press

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Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation

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Isoleucylation properties of native human mitochondrial tRNA Ile and tRNA Ile transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNA Ile gene

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Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA Ile mutation causing hypertrophic cardiomyopathy

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Mitochondrial tRNA Leu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation

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