1. Functional and molecular genetic analyses of nine newly identified XPD‐deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes. Issue 7 (25th June 2013) Authors: Schäfer, Annika; Gratchev, Alexei; Seebode, Christina; Hofmann, Lars; Schubert, Steffen; Laspe, Petra; Apel, Antje; Ohlenbusch, Andreas; Tzvetkov, Mladen; Weishaupt, Carsten; Oji, Vinzenz; Schön, Michael P.; Emmert, Steffen Journal: Experimental dermatology Issue: Volume 22:Issue 7(2013:Jul.) Page Start: 486 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗