A ribosomopathy reveals decoding defective ribosomes driving human dysmorphism. by Paolini, N, Attwood, M, Sondalle, S, Vieira, C, van Adrichem, A, di Summa, F, O'Donohue, M, Gleizes, P, Rachuri, S, Briggs, J, Fischer, R, Ratcliffe, P, Wlodarski, M, Houtkooper, R, von Lindern, M, Kuijpers, T, Dinman, J, Baserga, S, Cockman, M, MacInnes, A