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

By P. Laitinen, K. Brown, K. Piippo, H. Swan, J. Devaney, Bhoomi Brahmbhatt, E. A. Donarum, M. Marino, N. Tiso, M. Viitasalo and 3 more. Circulation, 2001

768 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/ec15669d2bcae44668945094fcee3345a175c9f7

How researchers see this paper

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In Cardiology and Cardiovascular Medicine

1. Bernard R. Chaitman
2. Rick A. Nishimura
3. J. Halperin
4. Jose Luis Zamorano
5. Douglas P. Zipes

In Molecular Biology

1. Douglas P. Zipes

Citations in the corpus

• ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: A report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (2006, background): “Half of the autosomal dominant cases are caused by mutations in the gene encoding the cardiac ryanodine receptor (RyR2), responsible for calcium release from the stores of the sarcoplasmic reticulum.(831,832) The recessive form is caused by mutations in the gene encoding calsequestrin (CASQ2), a cal”