1. Ahammed, Md Ripon, Ananya, Fariha Noor. 2023. Association of Cardiac Electrical Disorders With KCND3 Gene Mutation. In Cureus, 15, e34597. doi:10.7759/cureus.34597. https://pubmed.ncbi.nlm.nih.gov/36883079/
2. Teumer, Alexander, Trenkwalder, Teresa, Kessler, Thorsten, Behr, Elijah R, Reinhard, Wibke. 2019. KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern. In JCI insight, 4, . doi:10.1172/jci.insight.131156. https://pubmed.ncbi.nlm.nih.gov/31600170/
3. Li, Mengjie, Liu, Fen, Hao, Xiaoyan, Xu, Yuming, Shi, Changhe. 2022. Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22. In Frontiers in molecular neuroscience, 15, 919199. doi:10.3389/fnmol.2022.919199. https://pubmed.ncbi.nlm.nih.gov/35813061/
4. Gassanov, Natig, Er, Fikret, Michels, Guido, Brandt, Mathias C, Hoppe, Uta C. 2009. Divergent regulation of cardiac KCND3 potassium channel expression by the thyroid hormone receptors alpha1 and beta1. In The Journal of physiology, 587, 1319-29. doi:10.1113/jphysiol.2008.168385. https://pubmed.ncbi.nlm.nih.gov/19171649/
5. Wang, Jiaping, Wen, Yongxin, Zhang, Qingping, Zhang, YueHua, Bao, Xinhua. 2019. Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. In Seizure, 66, 26-30. doi:10.1016/j.seizure.2019.01.025. https://pubmed.ncbi.nlm.nih.gov/30776697/