1. Genetic variants as determinants of outcome in lamin A/C-related cardiac disease. (14th October 2021) Authors: Garcia Hernandez, S; Ortiz-Genga, M; Ochoa, J P; Lamounier, A; Fernandez, X; Cardenas, I; Garcia-Giustiniani, D; Brogger, M N; Fernandez, G; Valverde, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Marfan syndrome: genetic variant determinants of cardiovascular outcomes. (14th October 2021) Authors: Brogger, M N; Fernandez Ferro, G; Cardenas Reyes, I; Ochoa, J P; Garcia Hernandez, S; Fernandez, X; Garcia Giustiniani, D; Lamounier, A; Valverde, M; De La Higuera Romero, L; Ortiz Genga, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Molecular characterization of a cohort of individuals referred to genetic testing with suspected CPVT. (14th October 2021) Authors: Fernandez, G; Brogger, M.N; Garcia, S; Ochoa, J.P; De La Higuera, L; Fernandez, X; Garcia, D; Lamounier, A; Valverde, M; Cardenas Reyes, I; Ortiz, M; Monserrat, L; McKenna, W.J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Narrowing of the neonatal region in the FBN1 gene. (14th October 2021) Authors: Brogger, M N; Fernandez Ferro, G; Cardenas Reyes, I; Ochoa, J P; Garcia Hernandez, S; Valverde, M; Fernandez, X; Garcia Giustiniani, D; Lamounier, A; De La Higuera Romero, L; Ortiz Genga, M; Monserrat, L; McKenna, W J Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel Filamin C missense mutation associated with severe restrictive cardiomyopathy overlapping with left ventricular non-compaction. (25th November 2020) Authors: Garcia Hernandez, S; Ortiz-Genga, M; Analia Ramos, K; Ochoa, J.P; Lamounier, A; Fernandez, X; Cardenas, I; Garcia-Giustiniani, D; Brogger, M.N; Cicerchia, M.N; Fernandez, G; Monserrat, L Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Specific actin (ACTC1) missense variants are associated with different overlapping clinical phenotypes and outcomes. (14th October 2021) Authors: Valverde, M; Garcia Hernandez, S; Brogger, M N; Fernandez, G; Cardenas, I; Garcia-Gustiniani, D; Fernandez, X; Lamounier, A; Ochoa, J P; Ortiz-Genga, M; Monserrat, L; McKenna, W Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗