IndraLab

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CACNA1A activates FHM Type 1. 1 / 1

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"FHM Type 1, which accounts for around 50% of all FHM cases, is caused by mutations in the CACNA1A gene encoding the Ca v 2.1 P/Q voltage dependent calcium channel."

27199775

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IndraLab

Statements

CACNA1A activates FHM Type 1. 1 / 1

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