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Arch Ophthalmol. 1990;108(10):1407.

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1. Nikoskelainen EK, Savontaus ML, Wanne OP, Katila MJ, Nummelin KU. Leber's hereditary optic neuroretinopathy, a maternally inherited disease: a geneologic study in four pedigrees. Arch Ophthalmol. 1987;105:665-671. FREE FULL TEXT 2. Wallace DC, Singh G, Lott MT, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science. 1988;242:1427-1430. FREE FULL TEXT 3. Stone EM, Coppinger JM, Kardon RH, Donelson J. Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy. Arch Ophthalmol. 1990;108:1417-1420. FREE FULL TEXT 4. Johns DR. Improved molecular genetic diagnosis of Leber's hereditary optic neuropathy. N Engl J Med. 1990. In press. 5. Vilkki J, Savontaus M-L, Nikoskelainen EK. Genetic heterogeneity in Leber's hereditary optic neuropathy revealed by mitochondrial DNA polymorphism. Am J Hum Genet. 1989;45:206-211. PUBMED 6. Holt IJ, Miller DH, Harding AE. Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy. J Med Genet. 1989;26:739-743. FREE FULL TEXT 7. Lott MY, Voljavec AS, Wallace DC. Variable genotype of Leber's hereditary optic neuropathy patients. Am J Ophthalmol. 1990;109:625-631. PUBMED 8. Chen J-D, Cox I, Denton MJ. Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis. Hum Genet. 1989;82:203-207. PUBMED

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