Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene <i>CACNA1D</i> Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy.

Instead, mutant Cav1.3 L current density was reduced ( Figure 3 a,d), although this change did not reach statistical significance due to a larger current amplitude variation in cells transiently expressing wild-type Cav1.3 L channels ( Figure 3 e).

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