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MT-TL1

MT-TL1 is a mitochondrial gene. It is associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.

One common mutation is A3,243G. This mutation has been theorized to be associated with several other mitochondrial disease,[1] including diabetes mellitus and deafness.[2]

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Source: Wikipedia | The above article is available under the GNU FDL. | Edit this article


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