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2. Wissinger, Bernd, Schaich, Simone, Baumann, Britta, Zrenner, Eberhart, Kohl, Susanne. 2011. Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. In Human mutation, 32, 1398-406. doi:10.1002/humu.21580. https://pubmed.ncbi.nlm.nih.gov/21882291/
3. Alsalloum, Almaqdad, Mosin, Ilya, Shefer, Kristina, Mityaeva, Olga, Volchkov, Pavel. 2024. Novel and Previously Known Mutations of the KCNV2 Gene Cause Various Variants of the Clinical Course of Cone Dystrophy with Supernormal Rod Response in Children. In Journal of clinical medicine, 13, . doi:10.3390/jcm13164592. https://pubmed.ncbi.nlm.nih.gov/39200733/
4. Liu, Man, Zhu, Yingchuan, Huang, Lian, Lu, Yilu, Ma, Yongxin. 2021. Compound heterozygous KCNV2 variants contribute to cone dystrophy with supernormal rod responses in a Chinese family. In Molecular genetics & genomic medicine, 9, e1795. doi:10.1002/mgg3.1795. https://pubmed.ncbi.nlm.nih.gov/34535971/
5. Wu, Huimin, Cowing, Jill A, Michaelides, Michel, Hunt, David M, Webster, Andrew R. 2006. Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans. In American journal of human genetics, 79, 574-9. doi:. https://pubmed.ncbi.nlm.nih.gov/16909397/
6. Georgiou, Michalis, Robson, Anthony G, Fujinami, Kaoru, Héon, Elise, Michaelides, Michel. 2020. KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1. In American journal of ophthalmology, 225, 95-107. doi:10.1016/j.ajo.2020.11.022. https://pubmed.ncbi.nlm.nih.gov/33309813/
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