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Query Trace: Ophthalmoplegia and RRM2B[original query]

Mitochondrial DNA maintenance disorders in 102 patients from different parts of Russia: Mutational spectrum and phenotypes. Mitochondrion 2021 1 57 205-212. Bychkov I O, Itkis Y S, Tsygankova P G, Krylova T D, Mikhaylova S V, Klyushnikov S A, Pechatnikova N L, Degtyareva A V, Nikolaeva E A, Seliverstov Y A, Kurbatov S A, Dadali E L, Rudenskaya G E, Illarioshkin S N, Zakharova E Similar articles in PubMed
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 Similar articles in PubMed
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia. Brain : a journal of neurology 2014 Dec 137 (Pt 12): 3200-12. Horga Alejandro, Pitceathly Robert D S, Blake Julian C, Woodward Catherine E, Zapater Pedro, Fratter Carl, Mudanohwo Ese E, Plant Gordon T, Houlden Henry, Sweeney Mary G, Hanna Michael G, Reilly Mary Similar articles in PubMed