1. Teke, Mehmet Yasin, Citirik, Mehmet, Kabacam, Serkan, Demircan, Suleyman, Alikasifoglu, Mehmet. 2016. A novel missense mutation of the GRK1 gene in Oguchi disease. In Molecular medicine reports, 14, 3129-33. doi:10.3892/mmr.2016.5620. https://pubmed.ncbi.nlm.nih.gov/27511724/
2. Zhang, Houbin, Frederick, Jeanne M, Baehr, Wolfgang. . Unc119 gene deletion partially rescues the GRK1 transport defect of Pde6d (- /-) cones. In Advances in experimental medicine and biology, 801, 487-93. doi:10.1007/978-1-4614-3209-8_62. https://pubmed.ncbi.nlm.nih.gov/24664735/
3. Pak, Joseph S, Lee, Eun-Jin, Craft, Cheryl Mae. 2015. The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation. In Molecular vision, 21, 1281-94. doi:. https://pubmed.ncbi.nlm.nih.gov/26664249/
4. Hu, Hualei, Liu, Fei, Gao, Pan, Liu, Mugen, Ren, Xiang. 2024. Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases. In Frontiers in genetics, 15, 1409016. doi:10.3389/fgene.2024.1409016. https://pubmed.ncbi.nlm.nih.gov/39055259/
5. Zhang, Qingjiong, Zulfiqar, Fareeha, Riazuddin, S Amer, Riazuddin, Sheikh, Hejtmancik, J Fielding. 2005. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene. In Molecular vision, 11, 977-85. doi:. https://pubmed.ncbi.nlm.nih.gov/16319817/
6. Whitcomb, Tiffany, Sakurai, Keisuke, Brown, Bruce M, Kefalov, Vladimir J, Khani, Shahrokh C. 2009. Effect of g protein-coupled receptor kinase 1 (Grk1) overexpression on rod photoreceptor cell viability. In Investigative ophthalmology & visual science, 51, 1728-37. doi:10.1167/iovs.09-4499. https://pubmed.ncbi.nlm.nih.gov/19834036/
7. Oishi, Akio, Akimoto, Masayuki, Kawagoe, Naoaki, Takahashi, Masayo, Yoshimura, Nagahisa. . Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease. In American journal of ophthalmology, 144, 475-7. doi:. https://pubmed.ncbi.nlm.nih.gov/17765441/
8. Beltran, William A, Cideciyan, Artur V, Boye, Shannon E, Jacobson, Samuel G, Aguirre, Gustavo D. 2017. Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR Mutations. In Molecular therapy : the journal of the American Society of Gene Therapy, 25, 1866-1880. doi:10.1016/j.ymthe.2017.05.004. https://pubmed.ncbi.nlm.nih.gov/28566226/
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