P. Tintelen

A sodium-channel mutation causes isolated cardiac conduction disease

P. C. Viswanathan, A. Wilde, H. Tan, 2001, Nature.

OP-EHEA190679 1..16

M. Link, R. Hauer, L. Mestroni, 2019 .

evere cardiac phenotype with right ventricular predominance n a large cohort of patients with a single missense mutation in he DES gene

R. Hofstra, J. Saffitz, P. Tintelen, 2022 .

Scn5a mutation segregating with conduction abnormality but not with Brugada syndrome features in a family

C. Bezzina, A. Wilde, M. Mannens, 2000 .

Familial occurrence of isolated non‐compaction cardiomyopathy

R. Hauer, E. Vonken, A. Lorsheyd, 2006, European journal of heart failure.

Mortality of Inherited Arrhythmia Syndromes: Insight Into Their Natural History

A. Wilde, E. Sijbrands, M. Alders, 2012, Circulation. Cardiovascular genetics.

Relation between genotype and left-ventricular dilatation in patients with Marfan syndrome.

J. Osinga, G. Pals, J. Timmermans, 2014, Gene.

Homozygous premature truncation of the HERG protein : the human HERG knockout.

A. Wilde, T. Hoorntje, N. Sreeram, 1999, Circulation.

The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.

D. Judge, J. Mogensen, T. Šarić, 2015, European heart journal.

The prevalence of left and right bundle branch block morphology ventricular tachycardia amongst patients with arrhythmogenic cardiomyopathy and sustained ventricular tachycardia: insights from the European Survey on Arrhythmogenic Cardiomyopathy.

R. Hauer, L. Fauchier, E. Behr, 2021, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.