Disruption of an Atypical U12-type Minor Intron in SCN5A Causes Conduction Disease and Recurrent Ventricular Fibrillation
E. Singer(The University of Sydney), Robert Bagnall(The University of Sydney), C. Semsarian(The University of Sydney), Ginell Ranpura(The University of Sydney), Zachary Laksman(University of British Columbia), Jeremy S. Parker(University of British Columbia), Shiqi Li(nLIGHT (United States)), S. Fraser(Centenary Institute), Sungmin Lim(The University of Sydney)
Cited by 0
Related Papers
Modified lentiviral globin gene therapy for pediatric β0/β0 transfusion-dependent β-thalassemia: A single-center, single-arm pilot trial
|Cell stem cell|2024|77
Outcomes of the rehabilitative procedure for patients with pulmonary atresia, ventricular septal defect and hypoplastic pulmonary arteries beyond the infant period
|European Journal of Cardio-Thoracic Surgery|2014|29
Maturation of iPSC-derived cardiomyocytes in a heart-on-a-chip device enables modeling of dilated cardiomyopathy caused by R222Q-SCN5A mutation
|Biomaterials|2023|24
Clinical and genetic characteristics of familial hypercholesterolemia patients with type 2 diabetes
|Journal of Endocrinological Investigation|2018|15