1. A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction. Issue 10 (12th May 2017) Authors: Stallmeyer, Birgit; Kuß, Johanna; Kotthoff, Stefan; Zumhagen, Sven; Vowinkel, Kirsty; Rinné, Susanne; Matschke, Lina A.; Friedrich, Corinna; Schulze-Bahr, Ellen; Rust, Stephan; Seebohm, Guiscard; Decher, Niels; Schulze-Bahr, Eric Journal: Circulation research Issue: Volume 120:Issue 10(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome. Issue 5 (October 2015) Authors: Kuechler, Alma; Altmüller, Janine; Nürnberg, Peter; Kotthoff, Stefan; Kubisch, Christian; Borck, Guntram Journal: Molecular and cellular probes Issue: Volume 29:Issue 5(2015) Page Start: 330 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗