1. De Silva, Samantha R, Arno, Gavin, Robson, Anthony G, Webster, Andrew R, Mahroo, Omar A. 2020. The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies. In Progress in retinal and eye research, 82, 100898. doi:10.1016/j.preteyeres.2020.100898. https://pubmed.ncbi.nlm.nih.gov/32860923/
2. Pauzuolyte, Valda, Patel, Aara, Wawrzynski, James R, Steel, Karen P, Sowden, Jane C. 2023. Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease. In EMBO molecular medicine, 15, e17393. doi:10.15252/emmm.202317393. https://pubmed.ncbi.nlm.nih.gov/37642150/
3. Wawrzynski, James, Patel, Aara, Badran, Abdul, Henderson, Robert, Sowden, Jane C. 2022. Spectrum of Mutations in NDP Resulting in Ocular Disease; a Systematic Review. In Frontiers in genetics, 13, 884722. doi:10.3389/fgene.2022.884722. https://pubmed.ncbi.nlm.nih.gov/35651932/
4. Huang, Li, Zhang, Linyan, Li, Xiaoyu, Ding, Xiaoyan, Li, Zhan. 2022. Ocular manifestations of Chinese patients with copy number variants in the NDP gene. In Molecular vision, 28, 29-38. doi:. https://pubmed.ncbi.nlm.nih.gov/35656167/
5. Jiang, Keke, Wang, Shuying, Sun, Huixin, Gao, Rongyu, Zhang, Jie. 2023. Novel mutation in the NDP gene associated with Norrie disease in a Chinese pedigree. In Molecular genetics & genomic medicine, 12, e2345. doi:10.1002/mgg3.2345. https://pubmed.ncbi.nlm.nih.gov/38146894/