Mutations in two intracellular Ca2+ release channels or ryanodine receptors (RyR1 and RyR2) are associated with a number of human skeletal and cardiac diseases. This chapter discusses these diseases in terms of known mechanisms, controversies, and unanswered questions. We also compare the cardiac and skeletal muscle diseases to explore common mechanisms
CITATION STYLE
Durham, W. J., Wehrens, X. H. T., Sood, S., & Hamilton, S. L. (2007). Diseases associated with altered ryanodine receptor activity. Subcellular Biochemistry, 45, 273–321. https://doi.org/10.1007/978-1-4020-6191-2_10
Mendeley helps you to discover research relevant for your work.