Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
Open Access
- 1 February 1991
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 174 (3) , 1324-1330
- https://doi.org/10.1016/0006-291x(91)91567-v
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- The Molecular Genetics of Leber's Hereditary Optic NeuropathyArchives of Ophthalmology (1950), 1990
- Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1990
- A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator proteinNature, 1990
- Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNAGenomics, 1989
- The complete nucleotide sequence of theRattus norvegicus mitochondrial genome: Cryptic signals revealed by comparative analysis between vertebratesJournal of Molecular Evolution, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Leber's Hereditary Optic Neuroretinopathy, a Maternally Inherited DiseaseArchives of Ophthalmology (1950), 1987
- Complete sequence of bovine mitochondrial DNA conserved features of the mammalian mitochondrial genomeJournal of Molecular Biology, 1982
- Sequence and gene organization of mouse mitochondrial DNACell, 1981
- Sequence and organization of the human mitochondrial genomeNature, 1981