HuGE Literature Finder
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| 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 |
| Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort. Mitochondrion 2019 Sep . Heighton Julia N, Brady Lauren I, Sadikovic Bekim, Bulman Dennis E, Tarnopolsky Mark |
| 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 |
| The unfolding clinical spectrum of POLG mutations. Journal of medical genetics 2009 Nov 46 (11): 776-85. Blok M J, van den Bosch B J, Jongen E, Hendrickx A, de Die-Smulders C E, Hoogendijk J E, Brusse E, de Visser M, Poll-The B T, Bierau J, de Coo I F, Smeets H |
| Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population. Archives of neurology 2006 1 63 (1): 107-11. González-Vioque Emiliano, Blázquez Alberto, Fernández-Moreira Daniel, Bornstein Belén, Bautista Juan, Arpa Javier, Navarro Carmen, Campos Yolanda, Fernández-Moreno Miguel A, Garesse Rafael, Arenas Joaquin, Martín Miguel |
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