Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber’s hereditary optic neuropathy
- 1 July 2005
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 332 (2) , 614-621
- https://doi.org/10.1016/j.bbrc.2005.05.003
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Only male matrilineal relatives with Leber’s hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutationBiochemical and Biophysical Research Communications, 2005
- Gene MutationNeuromuscular Disorders, 2004
- Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese FamilyAmerican Journal of Human Genetics, 2004
- Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic NeuropathyAmerican Journal of Human Genetics, 2003
- Leber hereditary optic neuropathyJournal of Medical Genetics, 2002
- The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup JHuman Genetics, 2002
- Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutationsHuman Mutation, 1995
- Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1991
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981