1. 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/
2. Weisschuh, Nicole, Mazzola, Pascale, Bertrand, Miriam, Kohl, Susanne, Stingl, Katarina. 2021. Clinical Characteristics of POC1B-Associated Retinopathy and Assignment of Pathogenicity to Novel Deep Intronic and Non-Canonical Splice Site Variants. In International journal of molecular sciences, 22, . doi:10.3390/ijms22105396. https://pubmed.ncbi.nlm.nih.gov/34065499/
3. Durlu, Yusuf K, Köroğlu, Çiğdem, Tolun, Aslihan. . Novel recessive cone-rod dystrophy caused by POC1B mutation. In JAMA ophthalmology, 132, 1185-91. doi:10.1001/jamaophthalmol.2014.1658. https://pubmed.ncbi.nlm.nih.gov/24945461/
4. Kameya, Shuhei, Fujinami, Kaoru, Ueno, Shinji, Iwata, Takeshi, Tsunoda, Kazushige. . Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance. In Investigative ophthalmology & visual science, 60, 3432-3446. doi:10.1167/iovs.19-26650. https://pubmed.ncbi.nlm.nih.gov/31390656/
5. Jin, Xin, Chen, Lanlan, Wang, Dajiang, Chen, Zehua, Huang, Houbin. 2018. Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family. In Ophthalmic genetics, 39, 300-306. doi:10.1080/13816810.2018.1430239. https://pubmed.ncbi.nlm.nih.gov/29377742/
6. Alzahem, Tariq A, AlTheeb, Abdulwahab, Ba-Abbad, Rola. 2023. Phenotypic and genotypic features of POC1B-associated cone dystrophy. In Ophthalmic genetics, 45, 72-77. doi:10.1080/13816810.2023.2204361. https://pubmed.ncbi.nlm.nih.gov/37246743/
7. 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/