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Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

✍ Scribed by Kari Majamaa; Jukka S. Moilanen; Seija Uimonen; Anne M. Remes; Pasi I. Salmela; Mikko Kärppä; Kirsi A.M. Majamaa-Voltti; Harri Rusanen; Martti Sorri; Keijo J. Peuhkurinen; Ilmo E. Hassinen


Book ID
117852500
Publisher
American Society of Human Genetics
Year
1998
Tongue
English
Weight
96 KB
Volume
63
Category
Article
ISSN
0002-9297

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## Abstract ## Objective We studied the prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children in a defined population in Northern Ostrobothnia, Finland. ## Methods Children with diagnoses commonly associated with mitochondrial diseases were ascertained. Blo