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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

326 related items for PubMed ID: 16019721

  • 1. Mitochondrial DNA and disease.
    Dimauro S, Davidzon G.
    Ann Med; 2005; 37(3):222-32. PubMed ID: 16019721
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  • 2. Mitochondrial DNA mutations in human disease.
    DiMauro S, Schon EA.
    Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421
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  • 3. Mitochondrial DNA medicine.
    DiMauro S.
    Biosci Rep; 2007 Jun; 27(1-3):5-9. PubMed ID: 17484047
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  • 5. Mitochondrial DNA mutations in human disease.
    Greaves LC, Taylor RW.
    IUBMB Life; 2006 Mar; 58(3):143-51. PubMed ID: 16766381
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  • 14. 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; 28(2):89-96. PubMed ID: 18384291
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  • 17. Revealing the hidden complexities of mtDNA inheritance.
    White DJ, Wolff JN, Pierson M, Gemmell NJ.
    Mol Ecol; 2008 Dec; 17(23):4925-42. PubMed ID: 19120984
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  • 18. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.
    Finsterer J.
    Acta Neurol Scand; 2007 Jul; 116(1):1-14. PubMed ID: 17587249
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