1. Zeitz, Christina, Kloeckener-Gruissem, Barbara, Forster, Ursula, Munier, Francis L, Berger, Wolfgang. 2006. Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness. In American journal of human genetics, 79, 657-67. doi:. https://pubmed.ncbi.nlm.nih.gov/16960802/
2. Shi, Gang-An, Liang, Ming-Juan, Miao, Qin-Fei, Zhai, Qiong-Xiang, Chen, Zhi-Hong. 2024. CABP4 mutation in mice shows alteration in protein expression level and neuron discharge frequency. In Translational pediatrics, 13, 705-715. doi:10.21037/tp-23-484. https://pubmed.ncbi.nlm.nih.gov/38840676/
3. Guo, Yuxiong, Miao, Qinfei, Zhang, Yuxin, Zhai, Qiongxiang, Chen, Zhihong. . A novel missense creatine mutant of CaBP4, c.464G>A (p.G155D), associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), reduces the expression of CaBP4. In Translational pediatrics, 11, 396-402. doi:10.21037/tp-22-54. https://pubmed.ncbi.nlm.nih.gov/35378956/
4. Khan, Arif O, Alrashed, May, Alkuraya, Fowzan S. 2012. Clinical characterisation of the CABP4-related retinal phenotype. In The British journal of ophthalmology, 97, 262-5. doi:10.1136/bjophthalmol-2012-302186. https://pubmed.ncbi.nlm.nih.gov/23099293/
5. Fehlhaber, Katherine E, Majumder, Anurima, Boyd, Kimberly K, Fain, Gordon L, Sampath, Alapakkam P. 2023. A Novel Role for UNC119 as an Enhancer of Synaptic Transmission. In International journal of molecular sciences, 24, . doi:10.3390/ijms24098106. https://pubmed.ncbi.nlm.nih.gov/37175812/
6. Littink, Karin W, van Genderen, Maria M, Collin, Rob W J, Cremers, Frans P M, van den Born, L Ingeborgh. 2008. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder. In Investigative ophthalmology & visual science, 50, 2344-50. doi:10.1167/iovs.08-2553. https://pubmed.ncbi.nlm.nih.gov/19074807/
7. Chen, Zhi-Hong, Wang, Chun, Zhuo, Mu-Qing, Tang, Zhi-Hong, Zeng, Xiao-Lu. 2017. Exome sequencing identified a novel missense mutation c.464G>A (p.G155D) in Ca2+-binding protein 4 (CABP4) in a Chinese pedigree with autosomal dominant nocturnal frontal lobe epilepsy. In Oncotarget, 8, 78940-78947. doi:10.18632/oncotarget.20694. https://pubmed.ncbi.nlm.nih.gov/29108277/