Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation

Mutations in the Cardiac Ryanodine Receptor Gene ( <i>hRyR2</i> ) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia

Silvia G. Priori, Carlo Napolitano, Natascia Tiso et al. · Circulation · 2001 · 1.4K citations · Full text

Medicine, Cardiology, Genetics +16

Catecholaminergic Polymorphic Ventricular Tachycardia in Children

Antoine Leenhardt, V. Lucet, Isabelle Denjoy et al. · Circulation · 1995 · 1K citations

Medicine, Cardiology, Pediatrics +11

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Natascia Tiso · Human Molecular Genetics · 2001 · 806 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia

Päivi J. Laitinen, Kevin M. Brown, Kirsi Piippo et al. · Circulation · 2001 · 734 citations · Full text

Medicine, Cardiology, Genetics +16

Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje et al. · Circulation Research · 2002 · 400 citations · Full text

Medicine, Cardiology, Molecular Genetics +9