Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. (Nature genetics, 2010)

(untitled) - Haack, T; Danhauser, K; Haberberger, B; Hoser, J; Strecker, V; Boehm, D; Uziel, G; Lamantea, E; Invernizzi, F; Poulton, J; Rolinski, B; Iuso, A; et al.