1. Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome. Issue 12 (27th September 2022) Authors: Treimer, Ernestine; Kalayci, Tugba; Schumann, Sven; Suer, Ilknur; Greco, Sara; Schanze, Denny; Schmeisser, Michael J.; Kühl, Susanne J.; Zenker, Martin Journal: Human mutation Issue: Volume 43:Issue 12(2022) Page Start: 1866 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗