Caenorhabditis elegans, a pluricellular model organism to screen new genes involved in mitochondrial genome maintenance
Résumé
The inheritance of functional mitochondria depends on faithful replication and transmission of mitochondrial DNA (mtDNA). A large and heterogeneous group of human disorders is associated with mitochondrial genome quantitative and qualitative anomalies. Several nuclear genes have been shown to account for these severe OXPHOS disorders. However, in several cases the disease-causing mutations still remain unknown.
Origine : Fichiers produits par l'(les) auteur(s)
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