Leber's hereditary optic neuropathy and Kearns-Sayre syndrome: Mitochondrial DNA mutations
- 30 June 1991
- journal article
- Published by Elsevier in Survey of Ophthalmology
- Vol. 35 (6) , 463-472
- https://doi.org/10.1016/0039-6257(91)90110-2
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Leber's hereditary optic neuropathy in womenEye, 1990
- Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysisHuman Genetics, 1989
- URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase SubunitScience, 1986
- Mitochondrial morphometrics of histochemically identified human extraocular muscle fibersThe Anatomical Record, 1986
- NADH-CoQ REDUCTASE DEFICIENT MYOPATHY: SUCCESSFUL TREATMENT WITH RIBOFLAVINThe Lancet, 1983
- THIOSULPHATE-SULPHUR TRANSFERASE (RHODANESE) DEFICIENCY IN LEBER'S HEREDITARY OPTIC ATROPHYThe Lancet, 1981
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Organization and expression of the mammalian mitochondrial genome: a lesson in economyTrends in Biochemical Sciences, 1981
- Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblastsSomatic Cell and Molecular Genetics, 1981
- LEBER'S OPTIC NEUROPATHYBrain, 1979