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83. mtDNA mutations that cause optic neuropathy: how do we know? Howell N; Bogolin C; Jamieson R; Marenda DR; Mackey DA Am J Hum Genet; 1998 Jan; 62(1):196-202. PubMed ID: 9443868 [No Abstract] [Full Text] [Related]
84. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. Olsen NK; Hansen AW; Nørby S; Edal AL; Jørgensen JR; Rosenberg T Acta Neurol Scand; 1995 May; 91(5):326-9. PubMed ID: 7639060 [TBL] [Abstract][Full Text] [Related]
85. Mitochondrial DNA analysis in Leber's hereditary optic neuropathy. Barboni P; Mantovani V; Montagna P; Bragliani M; Cortelli P; Lugaresi E; Puddu P; Caramazza R Ophthalmic Paediatr Genet; 1992 Dec; 13(4):219-26. PubMed ID: 1488222 [TBL] [Abstract][Full Text] [Related]
86. Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case. Kerrison JB; Howell N; Miller NR; Hirst L; Green WR Ophthalmology; 1995 Oct; 102(10):1509-16. PubMed ID: 9097799 [TBL] [Abstract][Full Text] [Related]
87. A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy. Lamminen T; Majander A; Juvonen V; Wikström M; Aula P; Nikoskelainen E; Savontous ML Am J Hum Genet; 1995 May; 56(5):1238-40. PubMed ID: 7726182 [No Abstract] [Full Text] [Related]
88. Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. Riordan-Eva P; Harding AE J Med Genet; 1995 Feb; 32(2):81-7. PubMed ID: 7760326 [No Abstract] [Full Text] [Related]
89. Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy. Wissinger B; Besch D; Baumann B; Fauser S; Christ-Adler M; Jurklies B; Zrenner E; Leo-Kottler B Biochem Biophys Res Commun; 1997 May; 234(2):511-5. PubMed ID: 9177303 [TBL] [Abstract][Full Text] [Related]
90. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy. Jacobi FK; Leo-Kottler B; Mittelviefhaus K; Zrenner E; Meyer J; Pusch CM; Wissinger B Invest Ophthalmol Vis Sci; 2001 May; 42(6):1208-14. PubMed ID: 11328729 [TBL] [Abstract][Full Text] [Related]
91. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Newman NJ; Lott MT; Wallace DC Am J Ophthalmol; 1991 Jun; 111(6):750-62. PubMed ID: 2039048 [TBL] [Abstract][Full Text] [Related]
92. Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy. Yoneda M; Tsuji S; Yamauchi T; Inuzuka T; Miyatake T; Horai S; Ozawa T Lancet; 1989 May; 1(8646):1076-7. PubMed ID: 2566021 [No Abstract] [Full Text] [Related]
93. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy. Johns DR; Neufeld MJ Biochem Biophys Res Commun; 1993 Oct; 196(2):810-5. PubMed ID: 8240356 [TBL] [Abstract][Full Text] [Related]
94. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON. Rödel G; Laubhan R; Scheuerle A; Skowronek P; Haferkamp O Eur J Med Res; 1996 Jul; 1(10):491-4. PubMed ID: 9438147 [TBL] [Abstract][Full Text] [Related]
95. The two locus control of Leber hereditary optic neuropathy and a high penetrance in Japanese pedigrees. Nakamura M; Fujiwara Y; Yamamoto M Hum Genet; 1993 May; 91(4):339-41. PubMed ID: 8500789 [TBL] [Abstract][Full Text] [Related]
97. How rapidly does the human mitochondrial genome evolve? Howell N; Kubacka I; Mackey DA Am J Hum Genet; 1996 Sep; 59(3):501-9. PubMed ID: 8751850 [TBL] [Abstract][Full Text] [Related]
98. Low-penetrance branches in matrilineal pedigrees with Leber hereditary optic neuropathy. Howell N; Mackey DA Am J Hum Genet; 1998 Oct; 63(4):1220-4. PubMed ID: 9867707 [No Abstract] [Full Text] [Related]
99. Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations. Hofmann S; Bezold R; Jaksch M; Kaufhold P; Obermaier-Kusser B; Gerbitz KD Am J Hum Genet; 1997 Jun; 60(6):1539-42. PubMed ID: 9199577 [No Abstract] [Full Text] [Related]