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mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae

DNA polymerase γ (pol γ) is responsible for replication and repair of mitochondrial DNA (mtDNA). Over 150 mutations in POLG (which encodes pol γ) have been discovered in patients with mitochondrial disorders including Alpers, progressive external ophthalmoplegia and ataxia-neuropathy syndrome. Howev...

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Bibliografski detalji
Glavni autori: Stumpf, Jeffrey D., Bailey, Christopher M., Spell, Diana, Stillwagon, Matthew, Anderson, Karen S., Copeland, William C.
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2010
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2865372/
https://ncbi.nlm.nih.gov/pubmed/20185557
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq089
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