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Article

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

Annals of neurology - 1 Sept 2007

Uusimaa Johanna, Moilanen Jukka S, Vainionpää Leena, Tapanainen Päivi, Lindholm Päivi, Nuutinen Matti, Löppönen Tuija, Mäki-Torkko Elina, Rantala Heikki, Majamaa Kari

Abstract excerpt

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. Blood DNA from 522 s...

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PMID: 17823937
DOI: 10.1002/ana.21196

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17823937-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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