Several gene mutations in ryanodine receptors, affecting channel gating, have been associated with certain arrhythmias and cardiomyopathy. In this review, the authors highlight the role of the ryanodine receptor, a Ca2+-release channel, in the pathogenesis of fatal arrhythmia and heart failure. They discuss also the possibility of this receptor as a new therapeutic target.
- Masafumi Yano
- Takeshi Yamamoto
- Masunori Matsuzaki
