Pediatric Neurology Briefs (Oct 2007)

Phenotype of Mitochondrial DNA 3243A > G Mutation

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-21-10-7
Journal volume & issue
Vol. 21, no. 10
pp. 78 – 79

Abstract

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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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