Japanese case of diabetes mellitus and . deafness with mutation in mitochondrial tRNALeu(UUR)gene
- 15 May 1993
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 341 (8855) , 1291-1292
- https://doi.org/10.1016/0140-6736(93)91204-y
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAThe Lancet, 1992
- Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessNature Genetics, 1992
- Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionNature Genetics, 1992
- A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)Biochemical and Biophysical Research Communications, 1990
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990