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CACNA1S activates FPP. 1 / 1

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"31 Although approximately 10% of FPP patients remain genetically undefined, mutations in the skeletal muscle Ca 2 + channel (CACNA1S) or Na + channel (SCN4A) genes are known to cause FPP."

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IndraLab

Statements

CACNA1S activates FPP. 1 / 1

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