Novel Mitochondrial DNA Mutation in tRNALys(8296A → G) Associated with Diabetes
- 17 April 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 245 (2) , 523-527
- https://doi.org/10.1006/bbrc.1998.8437
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Mitochondrial diabetes mellitus: a reviewBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1995
- Diabetes With Mitochondrial Gene tRNALYS MutationDiabetes Care, 1994
- Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA Leu(UUR) geneDiabetes, 1994
- Mitochondrial diabetes mellitus: Prevalence and clinical characterization of diabetes due to mitochondrial tRNALeU(UUR) gene mutation in Japanese patientsDiabetologia, 1994
- A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNANew England Journal of Medicine, 1994
- 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
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.Proceedings of the National Academy of Sciences, 1985
- Sequence and organization of the human mitochondrial genomeNature, 1981