Phenotype of Mitochondrial DNA 3243A > G Mutation
Abstract
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.
DOI: https://doi.org/10.15844/pedneurbriefs-21-10-7 | Journal eISSN: 2166-6482
Language: English
Page range: 78 - 79
Published on: Oct 1, 2007
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2007 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.