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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijä: Copeland, William C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2008
Aiheet:
Linkit: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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