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CACNA1C-Q1916R activates SCD. 1 / 1

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"Here, we presented a rare large Chinese family with ER associated SCD, in which the disease phenotypes were mainly caused by a CACNA1C Q1916R mutation and modulated by the SCN5A-R1193Q variant and sex (XREF_FIG)."

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IndraLab

Statements

CACNA1C-Q1916R activates SCD. 1 / 1

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