1. Kschonsak, Marc, Chua, Han Chow, Weidling, Claudia, Pless, Stephan Alexander, Payandeh, Jian. 2021. Structural architecture of the human NALCN channelosome. In Nature, 603, 180-186. doi:10.1038/s41586-021-04313-5. https://pubmed.ncbi.nlm.nih.gov/34929720/
2. Bayat, Allan, Liu, Zhenjiang, Luo, Sheng, Liao, Weiping, Ren, Dejian. 2023. A new neurodevelopmental disorder linked to heterozygous variants in UNC79. In Genetics in medicine : official journal of the American College of Medical Genetics, 25, 100894. doi:10.1016/j.gim.2023.100894. https://pubmed.ncbi.nlm.nih.gov/37183800/
3. Chen, Hui-Wen, Ma, Chung-Pei, Chin, En, Huang, Po-Jung, Tan, Bertrand Chin-Ming. 2024. Imbalance in Unc80 RNA Editing Disrupts Dynamic Neuronal Activity and Olfactory Perception. In International journal of molecular sciences, 25, . doi:10.3390/ijms25115985. https://pubmed.ncbi.nlm.nih.gov/38892173/
4. Wie, Jinhong, Bharthur, Apoorva, Wolfgang, Morgan, Zhou, Yandong, Ren, Dejian. 2020. Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex. In Nature communications, 11, 3351. doi:10.1038/s41467-020-17105-8. https://pubmed.ncbi.nlm.nih.gov/32620897/
5. Shamseldin, Hanan E, Faqeih, Eissa, Alasmari, Ali, Gleeson, Joseph G, Alkuraya, Fowzan S. 2015. Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy. In American journal of human genetics, 98, 210-5. doi:10.1016/j.ajhg.2015.11.013. https://pubmed.ncbi.nlm.nih.gov/26708753/
6. Stenehjem, Kristen K, Schweigert, Jessica, Kumar, Parag. 2019. Atypical Presentation of Viral Gastroenteritis in a Three-year-old Child Due to a UNC80 Mutation. In Cureus, 11, e4395. doi:10.7759/cureus.4395. https://pubmed.ncbi.nlm.nih.gov/31223553/