1. Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis. Issue 4 (29th April 2016) Authors: Boppudi, S.; Bögershausen, N.; Hove, H.B.; Percin, E.F.; Aslan, D.; Dvorsky, R.; Kayhan, G.; Li, Y.; Cursiefen, C.; Tantcheva‐Poor, I.; Toft, P.B.; Bartsch, O.; Lissewski, C.; Wieland, I.; Jakubiczka, S.; Wollnik, B.; Ahmadian, M.R.; Heindl, L.M.; Zenker, M. Journal: Clinical genetics Issue: Volume 90:Issue 4(2016) Page Start: 334 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗