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5. Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms. Rahman S; Lake BD; Taanman JW; Hanna MG; Cooper JM; Schapira AH; Leonard JV Brain; 2000 Mar; 123 Pt 3():591-600. PubMed ID: 10686181 [TBL] [Abstract][Full Text] [Related]
6. Detection and quantification of point mutations in mitochondrial DNA by PCR. Yoneda M; Tanno Y; Tsuji S; Attardi G Methods Enzymol; 1996; 264():432-41. PubMed ID: 8965716 [No Abstract] [Full Text] [Related]
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11. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA. Graf WD; Sumi SM; Copass MK; Ojemann LM; Longstreth WT; Shanske S; Lombes A; DiMauro S Ann Neurol; 1993 Jun; 33(6):640-5. PubMed ID: 8388680 [TBL] [Abstract][Full Text] [Related]
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13. The molecular genetics of mitochondrial cytopathies: the Melbourne experience. Thyagarajan D; Byrne E; Dennet X; Marzuki S Clin Exp Neurol; 1992; 29():172-81. PubMed ID: 1343860 [TBL] [Abstract][Full Text] [Related]
14. The 3243 MELAS mutation in a pedigree with MERRF. Folgerø T; Torbergsen T; Oian P Eur Neurol; 1995; 35(3):168-71. PubMed ID: 7628497 [TBL] [Abstract][Full Text] [Related]
15. Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR. Moraes CT; Schon EA Methods Enzymol; 1996; 264():522-40. PubMed ID: 8965724 [No Abstract] [Full Text] [Related]
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17. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome. Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159 [TBL] [Abstract][Full Text] [Related]
18. [The correlation of the heteroplasmy of mtDNA and clinicopathological findings in the patients with mitochondrial encephalomyopathies]. Tanno Y; Tanaka K; Tsuji S Nihon Rinsho; 1997 Dec; 55(12):3270-6. PubMed ID: 9436449 [TBL] [Abstract][Full Text] [Related]
19. 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 [TBL] [Abstract][Full Text] [Related]
20. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype. Melone MA; Tessa A; Petrini S; Lus G; Sampaolo S; di Fede G; Santorelli FM; Cotrufo R Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]