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2. MRI findings in SANDO variety of the ataxia-neuropathy spectrum with a novel mutation in POLG (c.3287G>T): A case report. Parada-Garza JD; López-Valencia G; Miranda-García LA; Pérez-García G; Ruiz-Sandoval JL Neuromuscul Disord; 2020 Jul; 30(7):590-592. PubMed ID: 32600829 [TBL] [Abstract][Full Text] [Related]
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7. Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans. Baruffini E; Lodi T; Dallabona C; Puglisi A; Zeviani M; Ferrero I Hum Mol Genet; 2006 Oct; 15(19):2846-55. PubMed ID: 16940310 [TBL] [Abstract][Full Text] [Related]
8. Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study. Luoma P; Melberg A; Rinne JO; Kaukonen JA; Nupponen NN; Chalmers RM; Oldfors A; Rautakorpi I; Peltonen L; Majamaa K; Somer H; Suomalainen A Lancet; 2004 Sep 4-10; 364(9437):875-82. PubMed ID: 15351195 [TBL] [Abstract][Full Text] [Related]
9. Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population. González-Vioque E; Blázquez A; Fernández-Moreira D; Bornstein B; Bautista J; Arpa J; Navarro C; Campos Y; Fernández-Moreno MA; Garesse R; Arenas J; Martín MA Arch Neurol; 2006 Jan; 63(1):107-11. PubMed ID: 16401742 [TBL] [Abstract][Full Text] [Related]
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11. Genetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism. Sato K; Yabe I; Yaguchi H; Nakano F; Kunieda Y; Saitoh S; Sasaki H J Neurol; 2011 Jul; 258(7):1327-32. PubMed ID: 21301859 [TBL] [Abstract][Full Text] [Related]
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