The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome-like phenotype in mice.
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JCI Insight. 2023 Oct 23;8(20):e162100. doi: 10.1172/jci.insight.162100.
JCI Insight. 2023.
PMID: 37698939
Free PMC article.