Article Versions Notes

Rinné S, Stallmeyer B, Pinggera A, Netter MF, Matschke LA, Dittmann S, Kirchhefer U, Neudorf U, Opp J, Striessnig J, et al. Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy. International Journal of Molecular Sciences. 2022; 23(22):14215. https://doi.org/10.3390/ijms232214215

Rinné, Susanne, Birgit Stallmeyer, Alexandra Pinggera, Michael F. Netter, Lina A. Matschke, Sven Dittmann, Uwe Kirchhefer, Ulrich Neudorf, Joachim Opp, Jörg Striessnig, and et al. 2022. "Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy" International Journal of Molecular Sciences 23, no. 22: 14215. https://doi.org/10.3390/ijms232214215

Rinné, S., Stallmeyer, B., Pinggera, A., Netter, M. F., Matschke, L. A., Dittmann, S., Kirchhefer, U., Neudorf, U., Opp, J., Striessnig, J., Decher, N., & Schulze-Bahr, E. (2022). Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy. International Journal of Molecular Sciences, 23(22), 14215. https://doi.org/10.3390/ijms232214215