Cardiac Emerinopathy: A Non-syndromic Nuclear Envelopathy with Increased Risk of Thromboembolic Stroke due to Progressive Atrial Standstill and Left Ventricular Non-compaction

Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation

(2017) Akiko Seki et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

(2016) Roddy Walsh et al.   GENETICS IN MEDICINE

Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

(2016) Xavier Daumy et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics

(2014) Keisuke Abe et al.   Circulation-Arrhythmia and Electrophysiology

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications

(2012) Ingrid A.W. van Rijsingen et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction Cardiomyopathy

(2010) Yvonne M. Hoedemaekers et al.   Circulation-Cardiovascular Genetics

Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction

(2008) Sabine Klaassen et al.   CIRCULATION