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42. 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]
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47. 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]
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50. [A trial of molecular diagnosis in Leber's optic neuropathy]. Ara F; Hotta Y; Hayakawa M; Yanashima K; Kanai A; Fujiki K Nippon Ganka Gakkai Zasshi; 1991 Aug; 95(8):715-20. PubMed ID: 1950826 [TBL] [Abstract][Full Text] [Related]
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56. Leber's hereditary optic neuropathy: clinical and molecular genetic aspects. Preliminary results in our families. Van Caelenberghe E; Meire F; Broux C; Vassart G; Cochaux P Bull Soc Belge Ophtalmol; 1992; 243():139-46. PubMed ID: 1302143 [TBL] [Abstract][Full Text] [Related]
57. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy. Nakamura M Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918 [TBL] [Abstract][Full Text] [Related]
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