1. Tsai, Jhih-Jie, Hsu, Wen-Bin, Liu, Jia-Hua, Chang, Ching-Wen, Tang, Tang K. 2019. CEP120 interacts with C2CD3 and Talpid3 and is required for centriole appendage assembly and ciliogenesis. In Scientific reports, 9, 6037. doi:10.1038/s41598-019-42577-0. https://pubmed.ncbi.nlm.nih.gov/30988386/
2. Hoover, Amber N, Wynkoop, Aaron, Zeng, Huiqing, Niswander, Lee A, Liu, Aimin. 2008. C2cd3 is required for cilia formation and Hedgehog signaling in mouse. In Development (Cambridge, England), 135, 4049-58. doi:10.1242/dev.029835. https://pubmed.ncbi.nlm.nih.gov/19004860/
3. Cortés, Claudio R, McInerney-Leo, Aideen M, Vogel, Ida, Zankl, Andreas, Wicking, Carol. 2016. Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function. In Scientific reports, 6, 24083. doi:10.1038/srep24083. https://pubmed.ncbi.nlm.nih.gov/27094867/
4. Chang, Ching-Fang, Schock, Elizabeth N, O'Hare, Elizabeth A, Delany, Mary E, Brugmann, Samantha A. . The cellular and molecular etiology of the craniofacial defects in the avian ciliopathic mutant talpid2. In Development (Cambridge, England), 141, 3003-12. doi:10.1242/dev.105924. https://pubmed.ncbi.nlm.nih.gov/25053433/
5. Topa, Alexandra, Rohlin, Anna, Fehr, André, Bhatti-Søfteland, Madiha, Kölby, Lars. 2024. The value of genome-wide analysis in craniosynostosis. In Frontiers in genetics, 14, 1322462. doi:10.3389/fgene.2023.1322462. https://pubmed.ncbi.nlm.nih.gov/38318288/