Ataxia and cerebellar hypoexcitability in a mouse model of SCN1B-linked Dravet syndrome.

JCI Insight · 2025 · PMC12487675 · PMID 40923316

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approached significanceno p-value reported

WT ( P = 0.0004), while genotypic differences in ISI 40 ( P = 0.0781) and ISI 100 ( P = 0.00885) approached significance, suggesting preferential effects on transmitter release probability of CF terminals ( Figure 8C ).

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