Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene
- PMID: 8417984
- PMCID: PMC1205293
- DOI: 10.1093/genetics/133.1.133
Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene
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