1. Vetri, Luigi, Calì, Francesco, Vinci, Mirella, Romano, Valentino, Elia, Maurizio. 2020. A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy. In European journal of medical genetics, 63, 103848. doi:10.1016/j.ejmg.2020.103848. https://pubmed.ncbi.nlm.nih.gov/31972370/
2. Huo, Liang, Wu, Qiong, Yang, Fan, Yang, Zuozhen, Wang, Hua. 2023. Novel KCNC2 variant associated with developmental and epileptic encephalopathy. In International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 83, 357-367. doi:10.1002/jdn.10263. https://pubmed.ncbi.nlm.nih.gov/37203270/
3. Vetri, Luigi, Calì, Francesco, Vinci, Mirella, Romano, Valentino, Elia, Maurizio. 2020. Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy". In Neuropediatrics, 52, 153. doi:10.1055/s-0040-1716904. https://pubmed.ncbi.nlm.nih.gov/33111300/
4. Rademacher, Annika, Schwarz, Niklas, Seiffert, Simone, Weber, Yvonne, Muhle, Hiltrud. 2020. Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy. In Neuropediatrics, 51, 368-372. doi:10.1055/s-0040-1710524. https://pubmed.ncbi.nlm.nih.gov/32392612/
5. Hwang, Joo-Yeon, Lee, Hyo Jung, Go, Min Jin, Kim, Bong-Jo, Lee, Hye-Ja. 2016. An integrative study identifies KCNC2 as a novel predisposing factor for childhood obesity and the risk of diabetes in the Korean population. In Scientific reports, 6, 33043. doi:10.1038/srep33043. https://pubmed.ncbi.nlm.nih.gov/27623749/
6. Li, Lin, Liu, Zili, Yang, Haiyang, Hu, Jun, Shen, Xuefeng. 2022. Investigation of novel de novo KCNC2 variants causing severe developmental and early-onset epileptic encephalopathy. In Seizure, 101, 218-224. doi:10.1016/j.seizure.2022.09.004. https://pubmed.ncbi.nlm.nih.gov/36087422/
7. Wang, Sumei, Yu, Yejing, Wang, Xu, Gu, Weiyue, Sun, Dan. 2022. Emerging evidence of genotype-phenotype associations of developmental and epileptic encephalopathy due to KCNC2 mutation: Identification of novel R405G. In Frontiers in molecular neuroscience, 15, 950255. doi:10.3389/fnmol.2022.950255. https://pubmed.ncbi.nlm.nih.gov/36090251/
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