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CACNA1S inhibits hypoPP. 1 / 1

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"Familial hypoPP is caused by loss-of-function mutations in at least two different genes : CACNL1A3 and SCN4A encoding for the alpha1 subunits of the skeletal muscle L-type Ca 2+ channel and voltage de[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

17825556

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IndraLab

Statements

CACNA1S inhibits hypoPP. 1 / 1

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