1. Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome. Issue 2 (12th December 2018) Authors: Faridi, Rabia; Tona, Risa; Brofferio, Alessandra; Hoa, Michael; Olszewski, Rafal; Schrauwen, Isabelle; Assir, Muhammad Z.K.; Bandesha, Akhtar A.; Khan, Asma A.; Rehman, Atteeq U.; Brewer, Carmen; Ahmed, Wasim; Leal, Suzanne M.; Riazuddin, Sheikh; Boyden, Steven E.; Friedman, Thomas B. Journal: Human mutation Issue: Volume 40:Issue 2(2019) Page Start: 162 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗