1. Yanık, Özge, Batıoğlu, Figen, Sahin, Yavuz, Demirel, Sibel, Özmert, Emin. 2022. Seroreactivity against retinal proteins in a case of POC1B gene associated cone dystrophy with normal funduscopic appearance: a systematic approach to diagnosis. In Ophthalmic genetics, 44, 389-395. doi:10.1080/13816810.2022.2121842. https://pubmed.ncbi.nlm.nih.gov/36094084/
2. Zhang, Conghui, Zhang, Qi, Wang, Fang, Liu, Qin. 2015. Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish. In Biochemical and biophysical research communications, 465, 651-7. doi:10.1016/j.bbrc.2015.06.083. https://pubmed.ncbi.nlm.nih.gov/26188096/
3. Beck, Bodo B, Phillips, Jennifer B, Bartram, Malte P, Wolfrum, Uwe, Bolz, Hanno J. 2014. Mutation of POC1B in a severe syndromic retinal ciliopathy. In Human mutation, 35, 1153-62. doi:10.1002/humu.22618. https://pubmed.ncbi.nlm.nih.gov/25044745/