FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death

PKA Phosphorylation Dissociates FKBP12.6 from the Calcium Release Channel (Ryanodine Receptor)

Steven O. Marx, Steven Reiken, Yuji Hisamatsu et al. · Cell · 2000 · 2K citations · Full text

Life Sciences, Biochemistry, Cell Biology +16

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

Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Silvia G. Priori, Carlo Napolitano, Mirella Memmi et al. · Circulation · 2002 · 1.2K citations

Medicine, Cardiology, Genetics +13

Catecholaminergic Polymorphic Ventricular Tachycardia in Children

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

Medicine, Cardiology, Pediatrics +11

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

Peter J. Mohler, Jean‐Jacques Schott, Anthony O. Gramolini et al. · Nature · 2003 · 960 citations

Medicine, Cardiology, Genetics +15