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Journal Abstract Search

212 related items for PubMed ID: 16225398

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  • 5. A real-time ARMS PCR/high-resolution melt curve assay for the detection of the three primary mitochondrial mutations in Leber's hereditary optic neuropathy.
    Ryan SE, Ryan F, O'Dwyer V, Neylan D.
    Mol Vis; 2016; 22():1169-1175. PubMed ID: 27746671
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  • 6. Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.
    Genasetti A, Valentino ML, Carelli V, Vigetti D, Viola M, Karousou EG, Melzi d'Eril GV, De Luca G, Passi A, Pallotti F.
    J Mol Diagn; 2007 Sep; 9(4):538-45. PubMed ID: 17652639
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  • 12. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH, Tong Y, Li BH, Chen YK.
    Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
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  • 15. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I, Gabrilovac J, Bradvica M, Vidović T, Cerovski B, Fumić K, Boranić M.
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
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  • 16. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
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  • 20. [DNA diagnosis in the age of individual made-to-order medications].
    Mashima Y.
    Nippon Ganka Gakkai Zasshi; 2004 Dec; 108(12):863-85; discussion 886. PubMed ID: 15656090
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