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Inherited Mitochondrial Diseases of DNA Replication

Mitochondrial genetic diseases can result from defects in mitochondrial DNA (mtDNA) in the form of deletions, point mutations, or depletion, which ultimately cause loss of oxidative phosphorylation. These mutations may be spontaneous, maternally inherited, or a result of inherited nuclear defects in...

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Autor principal: Copeland, William C.
Format: Artigo
Idioma:Inglês
Publicat: 2008
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2271032/
https://ncbi.nlm.nih.gov/pubmed/17892433
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev.med.59.053006.104646
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