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Journal Abstract Search

148 related items for PubMed ID: 17276742

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  • 3. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
    Pang CY, Huang CC, Yen MY, Wang EK, Kao KP, Chen SS, Wei YH.
    J Formos Med Assoc; 1999 May; 98(5):326-34. PubMed ID: 10420700
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  • 7. Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies.
    Cao Y, Ma Y, Zhang Y, Li Y, Fang F, Wang S, Bu D, Xu Y, Pei P, Li L, Xiao Y, Wu H, Yang Y, Zou L, Qi Y.
    Mitochondrion; 2010 Jun; 10(4):330-4. PubMed ID: 20123042
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  • 9. Inheritance and expression of mitochondrial DNA point mutations.
    Holme E, Tulinius MH, Larsson NG, Oldfors A.
    Biochim Biophys Acta; 1995 May 24; 1271(1):249-52. PubMed ID: 7599216
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  • 11. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM.
    Lancet; 1996 Nov 09; 348(9037):1283-8. PubMed ID: 8909383
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  • 13. Investigation of common mitochondrial point mutations in Korea.
    Kwon SJ, Park SS, Kim JM, Ahn TB, Kim SH, Kim J, Lee SH, Ha CK, Ahn MY, Jeon BS.
    Ann N Y Acad Sci; 2004 Apr 09; 1011():339-44. PubMed ID: 15126311
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  • 14. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.
    Huang CC, Kuo HC, Chu CC, Liou CW, Ma YS, Wei YH.
    J Biomed Sci; 2002 Apr 09; 9(6 Pt 1):527-33. PubMed ID: 12372990
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  • 17. Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families.
    Uziel G, Moroni I, Lamantea E, Fratta GM, Ciceri E, Carrara F, Zeviani M.
    J Neurol Neurosurg Psychiatry; 1997 Jul 09; 63(1):16-22. PubMed ID: 9221962
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  • 18. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.
    Aust N Z J Med; 1994 Apr 09; 24(2):188-93. PubMed ID: 8042948
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