Phenotype of Mitochondrial DNA 3243A > G Mutation
The prevalence and common clinical manifestations of the mitochondrial DNA 3243A > G mutation in children in a defined population in Finland were studied at the Universities of Oulu and Turku and other centers.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2007-10-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/986 |