Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy
- 1 November 1991
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 88 (1) , 98-100
- https://doi.org/10.1007/bf00204937
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.1989
- Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysisHuman Genetics, 1989
- Mitochondrial DNA mutations and neuromuscular diseaseTrends in Genetics, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Maternal genes: mitochondrial diseases.1987
- The inheritance of Leber's diseaseActa Ophthalmologica, 1985
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.Proceedings of the National Academy of Sciences, 1977
- Leber's optic atrophy, a possible example of maternal inheritance.1972
- Leber's disease in the NetherlandsDocumenta Ophthalmologica, 1963