RSK2 mutation co‐segregates with X‐linked intellectual disability and attenuated Coffin–Lowry phenotype in a three‐generation family. (17th March 2013) - Maystadt, I; Destree, A; Benoit, V; Aeby, A; Lederer, D; Moortgat, S; Jurkiewicz, D; Krajewska‐Walasek, M; Hanauer, A; Thomas, GM