Disease Relevance of the So-Called Secondary Leber Hereditary Optic Neuropathy Mutations
- 30 June 1997
- journal article
- other
- Published by Elsevier in American Journal of Human Genetics
- Vol. 60 (6), 1539-1542
- https://doi.org/10.1016/s0002-9297(07)64248-7
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
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- Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON.1996
- Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.1996
- Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutationsHuman Mutation, 1995
- Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.1994
- Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4Nature Genetics, 1994
- Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.1993
- Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.1992
- Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1991