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Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice
Mutations in genes coding for mitochondrial helicases such as TWINKLE and DNA2 are involved in mitochondrial myopathies with mtDNA instability in both human and mouse. We show that inactivation of Pif1, a third member of the mitochondrial helicase family, causes a similar phenotype in mouse. pif1−/−...
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Gepubliceerd in: | Mitochondrion |
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Hoofdauteurs: | , , , , , , , , , , , , , , , |
Formaat: | Artigo |
Taal: | Inglês |
Gepubliceerd in: |
2016
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Onderwerpen: | |
Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5454384/ https://ncbi.nlm.nih.gov/pubmed/26923168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mito.2016.02.005 |
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