Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases
- 20 April 2007
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 355 (4), 1031-1037
- https://doi.org/10.1016/j.bbrc.2007.02.083
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- An Infant With a Mitochondrial A3243G Mutation Demonstrating the MELAS PhenotypePediatric Neurology, 2006
- Clinical and laboratory survey of 65 Chinese patients with Leigh syndromeChinese Medical Journal, 2006
- Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosisMitochondrion, 2006
- Clinical features of A3243G mitochondrial tRNA mutationBrain & Development, 2004
- Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes.Acta Neuropathologica, 2000
- The mitochondrial A3243G mutation presenting as severe cardiomyopathy.Journal of Medical Genetics, 1997
- The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.Journal of Neurology, Neurosurgery & Psychiatry, 1996
- Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNANeuromuscular Disorders, 1993
- Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessNature Genetics, 1992
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990