## 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
✦ LIBER ✦
Mitochondrial DNA Haplogroups Do Not Play a Role in the Variable Phenotypic Presentation of the A3243G Mutation
✍ Scribed by Antonio Torroni; Yolanda Campos; Chiara Rengo; Daniele Sellitto; Alessandro Achilli; Chiara Magri; Ornella Semino; Alberto García; Pilar Jara; Joaquín Arenas; Rosaria Scozzari
- Book ID
- 117854172
- Publisher
- American Society of Human Genetics
- Year
- 2003
- Tongue
- English
- Weight
- 220 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/373936
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