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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| Formato: | Livro |
| Publicado em: |
Pediatric Neurology Briefs Publishers,
2007-10-01T00:00:00Z.
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| Número de Chamada: |
A1234.567 |
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| Cópia 1 | Disponível |