Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
全外显子组测序发现Cav1.3基因CACNA1D中的杂合变异与家族性窦房结功能障碍和局灶性特发性癫痫相关
期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms232214215
Rinné, Susanne; Stallmeyer, Birgit; Pinggera, Alexandra; Netter, Michael F; Matschke, Lina A; Dittmann, Sven; Kirchhefer, Uwe; Neudorf, Ulrich; Opp, Joachim; Striessnig, Jörg; Decher, Niels; Schulze-Bahr, Eric