ALDH2 gene polymorphisms and metabolite alterations in the recurrence of atrial fibrillation after radiofrequency catheter ablations: a prospective and multicenter study
New phenotypic association for SMAD6 gene: its role in the development of cardiac conduction disorders and pulmonary arterial hypertension/hereditary haemorrhagic telangiectasia.
Therapeutic effect of selective serotonin reuptake inhibitors to gain-of-function KCND3 variant identified in a patient with early repolarization and refractory epilepsy.