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2. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy]. Wang Y; Tong Y; Hu SX; Wang JY; Shao JB; Zhang HX Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):397-400. PubMed ID: 17680528 [TBL] [Abstract][Full Text] [Related]
7. Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene. Leo-Kottler B; Christ-Adler M; Baumann B; Zrenner E; Wissinger B Ger J Ophthalmol; 1996 Jul; 5(4):233-40. PubMed ID: 8854108 [TBL] [Abstract][Full Text] [Related]
11. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families. Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial DNA mutations in Leber's optic neuropathy. Hurko O Ann Neurol; 1994 May; 35(5):636. PubMed ID: 7910006 [No Abstract] [Full Text] [Related]
13. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease. Sawano T; Tanaka M; Ohno K; Yoneda M; Ota Y; Terasaki H; Awaya S; Ozawa T Biochem Mol Biol Int; 1996 Apr; 38(4):693-700. PubMed ID: 8728098 [TBL] [Abstract][Full Text] [Related]
14. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy]. Toyo-Oka Y; Wada C; Yamabe H; Inoue M; Ishigaki M; Matsuyama N; Ohnuki Y; Ichibe Y; Wakakura M; Ohtani H Rinsho Byori; 1996 Jul; 44(7):676-80. PubMed ID: 8741498 [TBL] [Abstract][Full Text] [Related]
15. The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy. Cock HR; Tabrizi SJ; Cooper JM; Schapira AH Ann Neurol; 1998 Aug; 44(2):187-93. PubMed ID: 9708540 [TBL] [Abstract][Full Text] [Related]
16. High incidence of visual recovery among four Japanese patients with Leber's hereditary optic neuropathy with the 14484 mutation. Yamada K; Mashima Y; Kigasawa K; Miyashita K; Wakakura M; Oguchi Y J Neuroophthalmol; 1997 Jun; 17(2):103-7. PubMed ID: 9176781 [TBL] [Abstract][Full Text] [Related]
17. Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. Ferré M; Bonneau D; Milea D; Chevrollier A; Verny C; Dollfus H; Ayuso C; Defoort S; Vignal C; Zanlonghi X; Charlin JF; Kaplan J; Odent S; Hamel CP; Procaccio V; Reynier P; Amati-Bonneau P Hum Mutat; 2009 Jul; 30(7):E692-705. PubMed ID: 19319978 [TBL] [Abstract][Full Text] [Related]
18. [A molecular genetic study of Leber's disease]. Zhang LS Zhonghua Yan Ke Za Zhi; 1993 Mar; 29(2):103-4. PubMed ID: 8404350 [TBL] [Abstract][Full Text] [Related]
19. Fast capillary electrophoresis-laser induced fluorescence analysis of ligase chain reaction products: human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy. Muth J; Williams PM; Williams SJ; Brown MD; Wallace DC; Karger BL Electrophoresis; 1996 Dec; 17(12):1875-83. PubMed ID: 9034769 [TBL] [Abstract][Full Text] [Related]