Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.
- 1 November 1994
- Vol. 55 (5) , 1063-6
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Cytochrome c Oxidase Mutations in Leber Hereditary Optic NeuropathyBiochemical and Biophysical Research Communications, 1993
- The two locus control of Leber hereditary optic neurophathy and a high penetrance in Japanese pedigreesHuman Genetics, 1993
- No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHONFEBS Letters, 1992
- An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1992
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- Leber’s Hereditary Optic Neuroretinopathy and the X-Chromosomal Susceptibility Factor: No Linkage to DXS7Human Heredity, 1992
- Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1991
- Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.Journal of Medical Genetics, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Leber's disease in the NetherlandsDocumenta Ophthalmologica, 1963