1. Homozygous intronic MITF mutation causes severe Waardenburg syndrome type 2A. (6th September 2018) Authors: Rauschendorf, Marc‐Alexander; Zimmer, Andreas D.; Laut, Astrid; Demmer, Philipp; Rösler, Bernd; Happle, Rudolf; Sartori, Silvina; Fischer, Judith Journal: Pigment cell & melanoma research Issue: Volume 32:Number 1(2019) Page Start: 85 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗