The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific

N. Raule, F. Sevini, S. Li, A. Barbieri, F. Tallaro, L. Lomartire, D. Vianello, A. Montesanto, J.S. Moilanen, V. Bezrukov, H. Blanché, A. Hervonen, K. Christensen, L. Deiana, E.S. Gonos, T.B.L. Kirkwood, P. Kristensen, A. Leon, P.G. Pelicci, M. PoulainI.M. Rea, J. Remacle, J.M. Robine, S. Schreiber, E. Sikora, P. Eline Slagboom, L. Spazzafumo, M. Antonietta Stazi, O. Toussaint, J.W. Vaupel, G. Rose, K. Majamaa, M. Perola, T.E. Johnson, L. Bolund, H. Yang, G. Passarino, C. Franceschi

    Research output: Contribution to journalArticle

    54 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)401-407
    JournalAging Cell
    Volume13
    Issue number3
    DOIs
    Publication statusPublished - 17 Dec 2013

    Keywords

    • Genetics of longevity
    • Longevity
    • Mitochondrial DNA
    • MtDNA sequencing
    • Oxidative phosphorylation

    Cite this