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Authors: Anett Illés, Péter Balicza, Anikó Gál, Klára Pentelényi, Dóra Csabán, András Gézsi, Viktor Molnár and Mária Judit Molnár

; 82: 228–235. 3 Hsieh PC, Wang CC, Tsai CL, et al. POLG R964C and GBA L444P mutations in familial Parkinson’s disease: case

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Authors: András Szarka, Gábor Bánhegyi and Balázs Sümegi

Twinkle and polymerase POLG causes distinct replication stalling phenotypes. Nucl. Acids Res., 2007, 35 (10), 3238–3251. Balaban, R. S., Nemoto, S., Finkel, T., et al.: Mitochondria, oxidants, and aging. Cell, 2005

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Authors: Enikő Sáfrány, Veronika Csöngei, Luca Járomi, Anita Maász, Lili Magyari, Csilla Sipeky and Béla Melegh

Van Goethem, G., Dermaut, B., Lofgren, A. és mtsai: Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Nature Genetics, 2001, 28 , 211–212. Lofgren

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