1. Sun, Tengyang, Xu, Ke, Ren, Yanfan, Tian, Lu, Li, Yang. . Comprehensive Molecular Screening in Chinese Usher Syndrome Patients. In Investigative ophthalmology & visual science, 59, 1229-1237. doi:10.1167/iovs.17-23312. https://pubmed.ncbi.nlm.nih.gov/29625443/
2. Fuster-García, Carla, García-Bohórquez, Belén, Rodríguez-Muñoz, Ana, Millán, José M, García-García, Gema. 2021. Usher Syndrome: Genetics of a Human Ciliopathy. In International journal of molecular sciences, 22, . doi:10.3390/ijms22136723. https://pubmed.ncbi.nlm.nih.gov/34201633/
3. Ng, Natasha Hui Jin, Ghosh, Soumita, Bok, Chek Mei, Hoon, Shawn, Teo, Adrian Kee Keong. 2024. HNF4A and HNF1A exhibit tissue specific target gene regulation in pancreatic beta cells and hepatocytes. In Nature communications, 15, 4288. doi:10.1038/s41467-024-48647-w. https://pubmed.ncbi.nlm.nih.gov/38909044/
4. Tian, Cong, Liu, Xue Z, Han, Fengchan, Yan, Denise, Zheng, Qing Y. 2010. Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse. In Brain research, 1328, 57-70. doi:10.1016/j.brainres.2010.02.079. https://pubmed.ncbi.nlm.nih.gov/20211154/
5. Aparisi, María José, García-García, Gema, Jaijo, Teresa, Aller, Elena, Millán, José María. 2010. Novel mutations in the USH1C gene in Usher syndrome patients. In Molecular vision, 16, 2948-54. doi:. https://pubmed.ncbi.nlm.nih.gov/21203349/
6. Johnson, Kenneth R, Gagnon, Leona H, Webb, Lisa S, Chang, Bo, Zheng, Qing Yin. 2003. Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. In Human molecular genetics, 12, 3075-86. doi:. https://pubmed.ncbi.nlm.nih.gov/14519688/