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Genotype–phenotype correlation in the 5703G>A mutation in the tRNAAsngene of mitochondrial DNA

✍ Scribed by C. Vives-Bauza; M. Del Toro; A. Solano; J. Montoya; A. L. Andreu; M. Roig


Book ID
111548291
Publisher
Springer
Year
2003
Tongue
English
Weight
39 KB
Volume
26
Category
Article
ISSN
0141-8955

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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