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Journal Abstract Search

169 related items for PubMed ID: 15965049

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  • 6. [Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.].
    Chen G, Li W, DU WD, Cao HM, Tang HY, Tang XF, Sun ZW, Zhao H, Jin QH, Zhao JL, Zhang XJ.
    Yi Chuan; 2008 Oct; 30(10):1279-86. PubMed ID: 18930887
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  • 9. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J.
    Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
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  • 10. A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
    Vastagh I, Gál A, Reményi V, Semjén J, Lukács T, Valikovics A, Molnár MJ.
    Ideggyogy Sz; 2011 Nov 30; 64(11-12):399-403. PubMed ID: 22611618
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  • 11. The 3243 MELAS mutation in a pedigree with MERRF.
    Folgerø T, Torbergsen T, Oian P.
    Eur Neurol; 1995 Nov 30; 35(3):168-71. PubMed ID: 7628497
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  • 14. 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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  • 17. Heteroplasmic mitochondrial tRNA(Lys) mutation and its complementation in MERRF patient-derived mitochondrial transformants.
    Yoneda M, Miyatake T, Attardi G.
    Muscle Nerve Suppl; 1995 Apr 12; 3():S95-101. PubMed ID: 7603536
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  • 19. Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.
    Fan H, Civalier C, Booker JK, Gulley ML, Prior TW, Farber RA.
    J Mol Diagn; 2006 May 12; 8(2):277-81. PubMed ID: 16645216
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  • 20. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
    Campos Y, Garcia-Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J.
    Pediatr Neurol; 1995 Jul 12; 13(1):69-72. PubMed ID: 7575854
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