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Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
 
 
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Int. J. Mol. Sci. 2022, 23(22), 14216; https://doi.org/10.3390/ijms232214216
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