Japanese case of diabetes mellitus and . deafness with mutation in mitochondrial tRNALeu(UUR)gene
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA;Reardon;Lancet,1992
2. A point mutation in the mitochondrial tRNALeu(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes);Kobayashi;Biochem Biophys Res Commun,1990
3. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalopathies;Goto;Nature,1990
4. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness;van den Ouweland;Nature Genet,1992
5. Maternally transmitted diabetes and deafness associated with a 10-4 kb mitochondrial DNA deletion;Ballinger;Nature Genet,1992
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