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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

180 related items for PubMed ID: 12923421

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  • 2. Mitochondrial deafness.
    Kokotas H, Petersen MB, Willems PJ.
    Clin Genet; 2007 May; 71(5):379-91. PubMed ID: 17489842
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  • 3. Mitochondrial deafness mutations reviewed.
    Fischel-Ghodsian N.
    Hum Mutat; 1999 May; 13(4):261-70. PubMed ID: 10220138
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  • 8. Hearing loss in mitochondrial disorders.
    Hsu CH, Kwon H, Perng CL, Bai RK, Dai P, Wong LJ.
    Ann N Y Acad Sci; 2005 May; 1042():36-47. PubMed ID: 15965043
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  • 13. Molecular genetic and clinical aspects of mitochondrial disorders in childhood.
    Moslemi AR, Darin N.
    Mitochondrion; 2007 Jul; 7(4):241-52. PubMed ID: 17376748
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  • 17. [Diseases of the human mitochondrial oxidative phosphorylation system].
    Ruiz-Pesini E, López-Gallardo E, Dahmani Y, Herrero MD, Solano A, Díez-Sánchez C, López-Pérez M, Montoya J.
    Rev Neurol; 2007 Jul; 43(7):416-24. PubMed ID: 17006861
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  • 18. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
    Wallace DC.
    Gene; 2005 Jul 18; 354():169-80. PubMed ID: 16024186
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  • 20. Clinical and molecular findings in a patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene.
    Binder J, Hofmann S, Kreisel S, Wöhrle JC, Bäzner H, Krauss JK, Hennerici MG, Bauer MF.
    Brain; 2003 Aug 18; 126(Pt 8):1814-20. PubMed ID: 12805099
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