A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri–Weill dyschondrosteosis and Langer dysplasia. Issue 6 (1st June 2004) - Sabherwal, N; Blaschke, R J; Marchini, A; Heine-Suner, D; Rosell, J; Ferragut, J; Blum, W F; Rappold, G