REFERENCES
- Riordan-Eva P, Sanders M D, Govan G G, Sweeney M G, Da Costa J, Harding A E. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 1995; 118: 319–337, [PUBMED], [INFOTRIEVE], [CSA]
- Newman N J, Lott M T, Wallace D C. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol 1991; 111: 750–762, [PUBMED], [INFOTRIEVE], [CSA]
- Nakamura M, Yamamoto M. Variable pattern of visual recovery of Leber's hereditary optic neuropathy. Br J Ophthalmol 2000; 84: 534–535, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Stone E M, Newman N J, Miller N R, Johns D R, Lott M T, Wallace D C. Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation. J Clin Neuro-Ophthalmol 1992; 12: 10–14
- Mashima Y, Sato E A, Ohde H, Oguchi Y. Macular nerve fibers temporal to fovea may have a greater potential to recover function in patients with Leber's hereditary optic neuropathy. Jpn J Ophthalmol 2002; 46(6)660–667, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]