High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
Calvo 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 VK; Nature Genetics, 2010, vol. 42, issue 10, p 851, ISSN 15461718. ISBN 15461718.

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