IndraLab

Statements


Mutated SCN1A activates pyraclofos. 2 / 2
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"DS is an autosomal dominant disease that is mainly caused by various mutations of the SCN1A gene encoding the type 1 subunit of the neuronal voltage gated sodium channel [XREF_BIBR]."

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"Dravet syndrome is most frequently caused by various mutations of the SCN1A gene encoding the type 1 subunit of the neuronal voltage gated sodium channel."