1. 370 The CO-existence of KCNQ1 and TNNI3 genes mutations supports the genetic origin of QTC abnormalities in hypertrophic cardiomyopathy. (17th December 2020) Authors: Cava, Francesco; Cristiano, Ernesto; Lo Monaco, Maria; Musumeci, Maria Beatrice; Savio, Camilla; Petrucci, Simona; Rubattu, Speranza Donatella; Piane, Maria; Autore, Camillo Journal: European heart journal supplements Issue: Volume 22(2020)Supplement N Page Start: N83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗