Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome. (Clinical genetics, 2003)

(untitled) - Martínez-Garay, I; Ballesta, M; Oltra, S; Orellana, C; Palomeque, A; Moltó, MD; Prieto, F; Martínez, F