1. . . Editors' Note to: EDAR, LYPLAL1, PRDM16, PAX3, DKK1, TNFSF12, CACNA2D3, and SUPT3H gene variants influence facial morphology in a Eurasian population. In Human genetics, 139, 273. doi:10.1007/s00439-019-02097-3. https://pubmed.ncbi.nlm.nih.gov/31807863/
2. Bracic, Gerhard, Hegmann, Katrin, Engel, Jutta, Kurt, Simone. 2022. Impaired Subcortical Processing of Amplitude-Modulated Tones in Mice Deficient for Cacna2d3, a Risk Gene for Autism Spectrum Disorders in Humans. In eNeuro, 9, . doi:10.1523/ENEURO.0118-22.2022. https://pubmed.ncbi.nlm.nih.gov/35410870/
3. Shao, Wei, Zheng, Hang, Zhu, Jingwen, Wang, Kai, Jiang, Xiao. 2023. Deletions of Cacna2d3 in parvalbumin-expressing neurons leads to autistic-like phenotypes in mice. In Neurochemistry international, 169, 105569. doi:10.1016/j.neuint.2023.105569. https://pubmed.ncbi.nlm.nih.gov/37419212/
4. Wong, Alissa Michelle Go, Kong, Kar Lok, Chen, Leilei, Tsang, Janice Wing-hang, Guan, Xin-Yuan. 2013. Characterization of CACNA2D3 as a putative tumor suppressor gene in the development and progression of nasopharyngeal carcinoma. In International journal of cancer, 133, 2284-95. doi:10.1002/ijc.28252. https://pubmed.ncbi.nlm.nih.gov/23649311/
5. Wanajo, Aira, Sasaki, Akane, Nagasaki, Hiromi, Yuasa, Yasuhito, Akiyama, Yoshimitsu. 2008. Methylation of the calcium channel-related gene, CACNA2D3, is frequent and a poor prognostic factor in gastric cancer. In Gastroenterology, 135, 580-90. doi:10.1053/j.gastro.2008.05.041. https://pubmed.ncbi.nlm.nih.gov/18588891/
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