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4. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON). Peron C; Mauceri R; Cabassi T; Segnali A; Maresca A; Iannielli A; Rizzo A; Sciacca FL; Broccoli V; Carelli V; Tiranti V Stem Cell Res; 2020 Oct; 48():101939. PubMed ID: 32771908 [TBL] [Abstract][Full Text] [Related]
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