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3. Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome. Carreño-Gago L; Gamez J; Cámara Y; Alvarez de la Campa E; Aller-Alvarez JS; Moncho D; Salvado M; Galan A; de la Cruz X; Pinós T; García-Arumí E Biochim Biophys Acta Mol Basis Dis; 2017 Jan; 1863(1):182-187. PubMed ID: 27613247 [TBL] [Abstract][Full Text] [Related]
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