The mitochondrial DNA A3243G mutation in Werner's syndrome

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Experimental Gerontology, Vol. 38, Iss. 3, 2003-03 ,pp. : 339-342

Elsevier

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Comparison of the level of mitochondrial DNA A3243G mutation in esophageal epithelium and myocardium from individuals of very advanced age

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Experimental Gerontology, Vol. 37, Iss. 7, 2002-07 ,pp. : 917-923

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Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study

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Springer Publishing Company

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A Case of Melas (A3243G) on Chronic Dichloroacetate Treatment

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European Neurology, Vol. 55, Iss. 1, 2006-03 ,pp. : 37-38

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The mitochondrial theory of aging: Do damaged mitochondria accumulate by delayed degradation? - Demonstration of age-associated accumulation in human tissues of the A->G mutation at nucleotide 3243 in mitochondrial DNA

By Kowald A.  

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