Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. by Haack, T, Danhauser, K, Haberberger, B, Hoser, J, Strecker, V, Boehm, D, Uziel, G, Lamantea, E, Invernizzi, F, Poulton, J, Rolinski, B, Iuso, A, Biskup, S, Schmidt, T, Mewes, H, Wittig, I, Meitinger, T, Zeviani, M, Prokisch, H