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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. Poulain
  • I.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

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

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

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