Cardiovascular abnormalities in adult patients with the 3243A>G mutation in mitochondrial DNA
Abstract The 3243A>G mutation in mitochondrial DNA (mtDNA), the most common cause of the syndrome of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes, is also associated with many other phenotypes such as hearing loss, diabetes mellitus, epilepsy, cognitive decline, myop...
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| Format: | Doctoral Thesis |
| Language: | English |
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University of Oulu
2007
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| Online Access: | http://urn.fi/urn:isbn:9789514284304 http://nbn-resolving.de/urn:isbn:9789514284304 |