The sinoatrial node (SAN) is the primary pacemaker of the mammalian heart, initiating its
electrical activation and ensuring that the heart's functional cardiac output meets …

Atrial fibrillation (AF) is a globally prevalent cardiac arrhythmia with significant genetic
underpinnings, as highlighted by recent large-scale genetic studies. A prominent clinical …

Background A diagnosis of Lamin proteins A and C cardiomyopathy (LMNA-CM) not only
impacts disease prognosis, but also leads to specific guideline-recommended treatment …

Background Interatrial block (IAB) is a conduction delay in Bachmann's bundle with a well-
described association with structural heart disease, supraventricular arrhythmias, and …

The heritability of atrial fibrillation (AF) is well established. Over the last decade genetic
architecture of AF has been unraveled by genome-wide association studies and family …

The case report shares evidence for a better understanding of atrial standstill. This being a
rare arrhythmogenic condition. This is a 46-year-old woman presented with multiple sites of …

Aims This study aims to explore the presence of left ventricular (LV) and left atrial (LA)
morphological and functional abnormalities in patients with Barlow's disease (BD) without …

Variants in the lamin (LMNA) gene, responsible for encoding nuclear Lamin proteins A and
C, constitute a frequent cause of familial dilated cardiomyopathy (DCM) after titin (TTN) …

Genetic cardiomyopathies are hereditary cardiac diseases often diagnosed in young
patients and are characterized by live-threatening arrhythmias and heart failure. Among …

Background: Rare arrhythmia and cardiomyopathy gene variants have been associated with
all-cause mortality among individuals of European ancestry with atrial fibrillation (AF). The …