Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Ophthalmoplegia and POLG2[original query] |
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Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. Journal of neurology 2008 Sep 255 (9): 1384-91. Virgilio Roberta, Ronchi Dario, Hadjigeorgiou Georgios M, Bordoni Andreina, Saladino Francesca, Moggio Maurizio, Adobbati Laura, Kafetsouli Demetra, Tsironi Evangelia, Previtali Stefano, Papadimitriou Alexandros, Bresolin Nereo, Comi Giacomo |
Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging. Mitochondrion 2015 Dec 26 81-85. Paramasivam Arumugam, Meena Angamuthu Kannan, Pedaparthi Lalitha, Jyothi Vuskamalla, Uppin Megha S, Jabeen Shaikh Afshan, Sundaram Challa, Thangaraj Kumarasa |
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