1. Sangermano, Riccardo, Gupta, Priya, Price, Cherrell, Huckfeldt, Rachel M, Bujakowska, Kinga M. 2024. Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration. In Research square, , . doi:10.21203/rs.3.rs-3871956/v1. https://pubmed.ncbi.nlm.nih.gov/38405922/
2. Sangermano, Riccardo, Gupta, Priya, Price, Cherrell, Huckfeldt, Rachel M, Bujakowska, Kinga M. 2024. Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration. In NPJ genomic medicine, 9, 58. doi:10.1038/s41525-024-00439-3. https://pubmed.ncbi.nlm.nih.gov/39516462/
3. Wheway, Gabrielle, Schmidts, Miriam, Mans, Dorus A, Roepman, Ronald, Johnson, Colin A. 2015. An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. In Nature cell biology, 17, 1074-1087. doi:10.1038/ncb3201. https://pubmed.ncbi.nlm.nih.gov/26167768/
4. Borchert, Grace A, Shanks, Morag E, Whitfield, Jennifer, MacLaren, Robert E, Cehajic-Kapetanovic, Jasmina. 2024. Expanding the genotypic and phenotypic spectra with a novel variant in the ciliopathy gene, CFAP410, associated with selective cone degeneration. In Ophthalmic genetics, 45, 633-639. doi:10.1080/13816810.2024.2369271. https://pubmed.ncbi.nlm.nih.gov/39232248/
5. De Decker, Mathias, Zelina, Pavol, Moens, Thomas G, Pasterkamp, R Jeroen, Van Damme, Philip. 2024. C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis. In Brain : a journal of neurology, , . doi:10.1093/brain/awae331. https://pubmed.ncbi.nlm.nih.gov/39703094/