We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleHigh-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.AuthorsCalvo SE; Tucker EJ; Compton AG; Kirby DM; Crawford G; Burtt NP; Rivas M; Guiducci C; Bruno DL; Goldberger OA; Redman MC; Wiltshire E; Wilson CJ; Altshuler D; Gabriel SB; Daly MJ; Thorburn DR; Mootha VKPublicationNature genetics, 2010, Vol 42, Issue 10, p851ISSN1546-1718Publication typearticleDOI10.1038/ng.659