1. Lee, Yu-Ri, Thomas, Mervyn G, Roychaudhury, Arkaprava, Schwartz, Charles E, Kim, Cheol-Hee. 2023. Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability. In Research square, , . doi:10.21203/rs.3.rs-2683050/v1. https://pubmed.ncbi.nlm.nih.gov/36993381/
2. Töpf, Ana, Cox, Dan, Zaharieva, Irina T, Muntoni, Francesco, Straub, Volker. 2024. Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. In Nature genetics, 56, 395-407. doi:10.1038/s41588-023-01651-0. https://pubmed.ncbi.nlm.nih.gov/38429495/
3. Roychaudhury, Arkaprava, Lee, Yu-Ri, Choi, Tae-Ik, Schwartz, Charles E, Kim, Cheol-Hee. 2024. SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability. In Annals of neurology, 96, 914-931. doi:10.1002/ana.27037. https://pubmed.ncbi.nlm.nih.gov/39073169/
4. Xu, Yongjie, Yu, Wenmin, Xiong, Yuanzhu, Zuo, Bo, Feng, Xiaoting. 2010. Molecular characterization and expression patterns of serine/arginine-rich specific kinase 3 (SPRK3) in porcine skeletal muscle. In Molecular biology reports, 38, 2903-9. doi:10.1007/s11033-010-9952-1. https://pubmed.ncbi.nlm.nih.gov/20127522/
5. Nakagawa, Osamu, Arnold, Michael, Nakagawa, Masayo, Nishino, Ichizo, Olson, Eric N. . Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2. In Genes & development, 19, 2066-77. doi:. https://pubmed.ncbi.nlm.nih.gov/16140986/
6. Weng, Lingwei, Deng, Qingqing, Chen, Xiuli, Wang, Kai, Shao, Jie. . [A case of Congenital disorder of glycosylation due to SSR4 gene deletion]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 40, 364-367. doi:10.3760/cma.j.cn511374-20210918-00762. https://pubmed.ncbi.nlm.nih.gov/36854416/
7. Sharkova, Inna, Borovikov, Artem, Konovalov, Fedor, Kutsev, Sergey, Murtazina, Aysylu. 2024. Clinical and Genetic Analysis of Digenic Muscular Dystrophy due to SRPK3 and TTN Variants in Two Siblings. In Clinical genetics, , . doi:10.1111/cge.14673. https://pubmed.ncbi.nlm.nih.gov/39667923/
智鼠故事 
