Mitochondrial dysfunction as a cause of optic neuropathies
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- 1 January 2004
- journal article
- review article
- Published by Elsevier in Progress in Retinal and Eye Research
- Vol. 23 (1) , 53-89
- https://doi.org/10.1016/j.preteyeres.2003.10.003
Abstract
No abstract availableKeywords
This publication has 293 references indexed in Scilit:
- Leber's hereditary optic neuropathy with 14484 mutation in Central Java, IndonesiaJournal of Human Genetics, 2003
- Leber hereditary optic neuropathy: A nuclear solution of a mitochondrial problemAnnals of Neurology, 2002
- Biochemical features of mtDNA 14484 (ND6/m64V) point mutation associated with Leber's hereditary optic neuropathyAnnals of Neurology, 1999
- Identification of a Fission Yeast Dynamin-Related Protein Involved in Mitochondrial DNA MaintenanceBiochemical and Biophysical Research Communications, 1998
- Mutation Analysis of the ND6 Gene in Patients with Lebers Hereditary Optic NeuropathyBiochemical and Biophysical Research Communications, 1997
- The mitochondrial permeability transitionBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1995
- Cytochrome c Oxidase Mutations in Leber Hereditary Optic NeuropathyBiochemical and Biophysical Research Communications, 1993
- The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathyHuman Genetics, 1993
- An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1992
- Cytochrome b mutations in Leber hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1991