Phenotype of Mitochondrial DNA 3243A > G Mutation

The prevalence and common clinical manifestations of the mitochondrial DNA 3243A > G mutation in children in a defined population in Finland were studied at the Universities of Oulu and Turku and other centers.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awdur: J Gordon Millichap (Awdur)
Fformat: Llyfr
Cyhoeddwyd: Pediatric Neurology Briefs Publishers, 2007-10-01T00:00:00Z.
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3rd Floor Main Library

Manylion daliadau o 3rd Floor Main Library
Rhif Galw: A1234.567
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