J.U. and J.S.M. contributed equally to this work.
Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children
Version of Record online: 6 SEP 2007
Copyright © 2007 American Neurological Association
Annals of Neurology
Volume 62, Issue 3, pages 278–287, September 2007
How to Cite
Uusimaa, J., Moilanen, J. S., Vainionpää, L., Tapanainen, P., Lindholm, P., Nuutinen, M., Löppönen, T., Mäki-Torkko, E., Rantala, H. and Majamaa, K. (2007), Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children. Ann Neurol., 62: 278–287. doi: 10.1002/ana.21196
- Issue online: 25 SEP 2007
- Version of Record online: 6 SEP 2007
- Manuscript Accepted: 25 JUN 2007
- Manuscript Revised: 13 JUN 2007
- Manuscript Received: 28 DEC 2006
- Arvo and Lea Ylppö Foundation
- Foundation for Pediatric Research
- Medical Research Council of the Academy of Finland (decisions). Grant Numbers: 107490, 108953, 54289, 68104, 79843
- Sigrid Juselius Foundation
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