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3. Association in the same patient of autosomal dominant progressive external ophthalmoplegia with multiple mtDNA deletions and X-linked ichthyosis: clinical, biochemical, histological, submicroscopic and molecular genetic study. Federico A, Dotti MT, Cardaioli E, Grieco G, Malandrini A, Manneschi L, Plewnia K, Rufa A, Renieri A, Bruttini M, Perticoni GF. J Submicrosc Cytol Pathol; 1998 Oct; 30(4):521-6. PubMed ID: 9851061 [Abstract] [Full Text] [Related]
5. [A single deletion of mitochondrial DNA in a Brazilian patient with chronic progressive external ophthalmoplegia]. Carod-Artal FJ, Solano-Palacios A, Playán-Ariso A, Viana-Brandi I, López-Gallardo E, Andreu A, López-Pérez M, Montoya J. Rev Neurol; 1998 Oct; 37(11):1029-31. PubMed ID: 14669142 [Abstract] [Full Text] [Related]
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11. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Van Goethem G, Dermaut B, Löfgren A, Martin JJ, Van Broeckhoven C. Nat Genet; 2001 Jul; 28(3):211-2. PubMed ID: 11431686 [Abstract] [Full Text] [Related]
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19. [Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies]. Laforêt P, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M, Lombès A. Rev Neurol (Paris); 1997 Feb; 153(1):51-8. PubMed ID: 9296156 [Abstract] [Full Text] [Related]