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

Author(s):
Raule, N.; Sevini, F.; Li, S.T.; Barbieri, A.; Tallaro, F.; Lomartire, L.; Vianello, D.; Montesanto, A.; Moilanen, J.S.; Bezrukov, V.; Blanche, H.; Hervonen, A.; Christensen, K.; Deiana, L.; Gonos, E.S.; Kirkwood, T.B.L.; Kristensen, P.; Leon, A.; Pelicci, P.G.; Poulain, M.; Rea, I.M.; Remacle, J.; Robine, J.M.; Schreiber, S.; Sikora, E.; Slagboom, P.E.; Spazzafumo, L.; Stazi, M.A.; Toussaint, O.; Vaupel, J.W.; Rose, G.; Majamaa, K.; Perola, M.; Johnson, T.E.; Bolund, L.; Yang, H.M.; Passarino, G.; Franceschi, C.
Published
2014
Publication type
Article / Letter to editor
genetics of longevitylongevitymitochondrial DNAmtDNA sequencingoxidative phosphorylation
Date issued
2014-06-30
Language
English
Is part of
Aging Cell (2014), Vol. 13, no. 3, p. 401-407
hdl
1887/107126
doi
10.1111/acel.12186