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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 7525879

  • 1. Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO).
    Hattori Y, Goto Y, Sakuta R, Nonaka I, Mizuno Y, Horai S.
    J Neurol Sci; 1994 Aug; 125(1):50-5. PubMed ID: 7525879
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  • 2. A novel heteroplasmic tRNA(Leu(CUN)) mtDNA point mutation associated with chronic progressive external ophthalmoplegia.
    Cardaioli E, Da Pozzo P, Radi E, Dotti MT, Federico A.
    Biochem Biophys Res Commun; 2005 Feb 18; 327(3):675-8. PubMed ID: 15649400
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  • 4. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
    Kornblum C, Zsurka G, Wiesner RJ, Schröder R, Kunz WS.
    Biosci Rep; 2008 Apr 18; 28(2):89-96. PubMed ID: 18384291
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  • 7. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.
    Houshmand M, Larsson NG, Holme E, Oldfors A, Tulinius MH, Andersen O.
    Biochim Biophys Acta; 1994 Apr 12; 1226(1):49-55. PubMed ID: 8155739
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  • 13. A novel mitochondrial tRNA(Val) T1658C mutation identified in a CPEO family.
    Yan N, Cai S, Guo B, Mou Y, Zhu J, Chen J, Zhang T, Li R, Liu X.
    Mol Vis; 2010 Aug 25; 16():1736-42. PubMed ID: 20806033
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  • 14. A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis.
    Taylor RW, Chinnery PF, Bates MJ, Jackson MJ, Johnson MA, Andrews RM, Turnbull DM.
    Biochem Biophys Res Commun; 1998 Feb 04; 243(1):47-51. PubMed ID: 9473477
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  • 15. Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging.
    Paramasivam A, Meena AK, Pedaparthi L, Jyothi V, Uppin MS, Jabeen SA, Sundaram C, Thangaraj K.
    Mitochondrion; 2016 Jan 04; 26():81-5. PubMed ID: 26689116
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  • 16. A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia.
    Spagnolo M, Tomelleri G, Vattemi G, Filosto M, Rizzuto N, Tonin P.
    Neuromuscul Disord; 2001 Jul 04; 11(5):481-4. PubMed ID: 11404121
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  • 19. A new mitochondrial point mutation in the transfer RNA(Lys) gene associated with progressive external ophthalmoplegia with impaired respiratory regulation.
    Wolf J, Obermaier-Kusser B, Jacobs M, Milles C, Mörl M, von Pein HD, Grau AJ, Bauer MF.
    J Neurol Sci; 2012 May 15; 316(1-2):108-11. PubMed ID: 22326363
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  • 20. Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA.
    Thajeb P, Ma YS, Tzen CY, Chuang CK, Wu TY, Chen SC, Wei YH.
    Clin Neurol Neurosurg; 2006 Jun 15; 108(4):407-10. PubMed ID: 16644408
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