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 journalArticlepeer-review

87 Citations (Scopus)
Original languageEnglish
Pages (from-to)401-407
JournalAging Cell
Volume13
Issue number3
DOIs
Publication statusPublished (in print/issue) - 17 Dec 2013

Bibliographical note

cited By 28

Keywords

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

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