1. Chen, Saipeng, Xiao, Longfei, Peng, Huahong, Wang, Zhen, Xie, Jianbing. 2021. Methylation gene KCNC1 is associated with overall survival in patients with seminoma. In Oncology reports, 45, . doi:10.3892/or.2021.8024. https://pubmed.ncbi.nlm.nih.gov/34105734/
2. Poirier, Karine, Viot, Géraldine, Lombardi, Laura, Billuart, Pierre, Bienvenu, Thierry. 2017. Loss of Function of KCNC1 is associated with intellectual disability without seizures. In European journal of human genetics : EJHG, 25, 560-564. doi:10.1038/ejhg.2017.3. https://pubmed.ncbi.nlm.nih.gov/28145425/
3. Spinelli, Sara, Remigante, Alessia, Liuni, Raffaella, Morabito, Rossana, Dossena, Silvia. 2024. Oxidative stress-related cellular aging causes dysfunction of the Kv3.1/KCNC1 channel reverted by melatonin. In Aging cell, 23, e14185. doi:10.1111/acel.14185. https://pubmed.ncbi.nlm.nih.gov/38725150/
4. Qiuju, He, Jianlong, Zhuang, Qi, Wen, Xiaofang, Sun, Yingjun, Xie. 2022. Epilepsy Combined With Multiple Gene Heterozygous Mutation. In Frontiers in pediatrics, 10, 763642. doi:10.3389/fped.2022.763642. https://pubmed.ncbi.nlm.nih.gov/35299674/
5. Cameron, Jillian M, Maljevic, Snezana, Nair, Umesh, Petrou, Steven, Berkovic, Samuel F. 2019. Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations. In Annals of clinical and translational neurology, 6, 1263-1272. doi:10.1002/acn3.50822. https://pubmed.ncbi.nlm.nih.gov/31353855/
6. Muona, Mikko, Berkovic, Samuel F, Dibbens, Leanne M, Palotie, Aarno, Lehesjoki, Anna-Elina. 2014. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. In Nature genetics, 47, 39-46. doi:10.1038/ng.3144. https://pubmed.ncbi.nlm.nih.gov/25401298/