Werner, Hauke Neurogenetics, Max Planck Institute of Experimental Medicine, Max Planck Society;
Brendel_10.pdf (Verlagsversion), 768KB
Brendel, C., Belakhov, V., Werner, H., Wegener, E., Gärtner, J., Nudelman, I., et al. (2011). Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. Journal of Molecular Medicine, 89, 389-398. doi:10.1007/s00109-010-0704-4.
