High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

✍ Scribed by Calvo, Sarah E; Tucker, Elena J; Compton, Alison G; Kirby, Denise M; Crawford, Gabriel; Burtt, Noel P; Rivas, Manuel; Guiducci, Candace; Bruno, Damien L; Goldberger, Olga A

• Book ID: 109914657
• Publisher: Nature Publishing Group
• Year: 2010
• Tongue: English
• Weight: 602 KB
• Volume: 42
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng.659