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SCN1A activates FHM3 subtype. 1 / 1

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"The FHM3 subtype is caused by mutations in SCN1A, which is also the most frequent epilepsy gene encoding the voltage gated Na + channel Na V 1.1."

26763045

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IndraLab

Statements

SCN1A activates FHM3 subtype. 1 / 1

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