1)井街 譲:レーベル氏病,附 優性型幼児性視神経萎縮症.日眼会誌77:1658-1735,1973
2)Hotta Y et al:Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA. Jpn J Ohthalmol 39:96-108, 1995
3)Ueda K et al:Nationwide epidemiological survey of Leber hereditary optic neuropathy in Japan. J Epidemiol 27:447-450, 2017
4)Takano F et al:Incidence of Leber hereditary optic neuropathy in 2019 in Japan:a second nationwide questionnaire survey. Orphanet J Rare Dis. doi:10.1186/s13023-022-02478-4, 2022
5)Godefrooij DA et al:Age-specific incidence and prevalence of keratoconus:a nationwide registration study. Am J Ophthalmol 175:169-172, 2017
6)Mackey DA et al:Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy. Am J Hum Genet 59:481-485, 1996
7)Yu-Wai-Man P et al:The epidemiology of Leber hereditary optic neuropathy in the North East of England. Am J Hum Genet 72:333-339, 2003
8)Puomila A et al:Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland. Eur J Hum Genet 15:1079-1089, 2007
9)Rosenberg T et al:Prevalence and genetics of Leber hereditary optic neuropathy in the Danish population. Invest Ophthalmol Vis Sci 57:1370-1375, 2016
10)岩佐真弓・他:高齢発症のレーベル遺伝性視神経症14症例の検討.神経眼科35:55-58,2018
11)Sadun AA et al:A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy. Trans Am Ophthalmol Soc 100:169-178, 2002
12)Vestergaard N et al:Increased mortality and comorbidity associated with Leber's hereditary optic neuropathy:a nationwide cohort study. Invest Ophthalmol Vis Sci 58:4586-4592, 2017