Leber's hereditary optic neuropathy among Japanese
- 1 January 1995
- journal article
- case report
- Published by Wiley in Muscle & Nerve
- Vol. 18 (S14) , S85-S89
- https://doi.org/10.1002/mus.880181418
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.Proceedings of the National Academy of Sciences, 1994
- Cytochrome c Oxidase Mutations in Leber Hereditary Optic NeuropathyBiochemical and Biophysical Research Communications, 1993
- Leber's Hereditary Optic NeuropathyArchives of Ophthalmology (1950), 1993
- Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1990
- Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.Journal of Medical Genetics, 1989
- 31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.Proceedings of the National Academy of Sciences, 1984
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Maternal inheritance of human mitochondrial DNA.Proceedings of the National Academy of Sciences, 1980
- A New VideopupillographyOphthalmologica, 1970
- A probable case of cytoplasmic inheritance in man: A critique of leber’s diseaseJournal of Genetics, 1936