Novel regulators of RyR Ca(2+) release channels: insight into molecular changes in genetically-linked myopathies
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Authors
Dulhunty, Angela
Beard, Nicole
Pouliquin, Pierre
Kimura, Takashi
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Springer
Abstract
There are many mutations in the ryanodine receptor (RyR) Ca2+ release channel that are implicated in skeletal muscle disorders and cardiac arrhythmias. More than 80 mutations in the skeletal RyR1 have been identified and linked to malignant hyperthermia,
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Journal of Muscle Research and Cell Motility
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Restricted until
2037-12-31