Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome. (21st December 2018) - Ulrich, Maximilian; Tinschert, Sigrid; Siebert, Eberhard; Franke, Ingolf; Tüting, Thomas; Ulrich, Jens; Schanze, Denny; Wieland, Ilse; Zenker, Martin