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Do not flush supplements down the toilet, as this can contaminate the water supply
Immunoblot of indicated proteins in HeLa SLC25A39 knockout cells expressing indicated cDNAs (bottom)
Genetic Basis and Pathophysiology Most cases of MH are associated with mutations in the RYR1 gene , which encodes the ryanodine receptor type 1 (RyR1) calcium-release channel in skeletal muscle
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