IndraLab

Statements

CACNA1A activates FHM type 1. 2 / 2
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"FHM type 1 (FHM1) is caused by missense mutations in the CACNA1A gene (e.g., R192Q, S218L) encoding the pore forming alpha 1A subunit of neuronal voltage gated Ca V 2.1 channels."
21490217
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"FHM type 1 (FHM1) is caused by mutations in the CACNA1A gene, which encodes the pore forming alpha 1A subunit of neuronal Ca V 2.1 voltage gated Ca 2+ channels 9."
22144569