1. Wu, Ruohao, Tang, Wenting, Qiu, Kunyin, Li, Xiaojuan, He, Zhanwen. . [Analysis of SSR4 gene variant in a child with congenital glycosylation type 1y in conjunct with congenital dysplasia of external auditory canal]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 39, 727-730. doi:10.3760/cma.j.cn511374-20210205-00114. https://pubmed.ncbi.nlm.nih.gov/35810430/
2. Shao, Wei, Cai, Qing, Tong, Sen-Miao, Ying, Sheng-Hua, Feng, Ming-Guang. 2020. Nuclear Ssr4 Is Required for the In Vitro and In Vivo Asexual Cycles and Global Gene Activity of Beauveria bassiana. In mSystems, 5, . doi:10.1128/mSystems.00677-19. https://pubmed.ncbi.nlm.nih.gov/32317391/
3. He, Weiwei, Wang, Bin, He, Jikai, Zhao, Youcai, Zhao, Wei. 2021. SSR4 as a prognostic biomarker and related with immune infiltration cells in colon adenocarcinoma. In Expert review of molecular diagnostics, 22, 223-231. doi:10.1080/14737159.2022.2019015. https://pubmed.ncbi.nlm.nih.gov/34904499/
4. Wang, Jun, Gou, Xingqing, Wang, Xiyi, Zhao, Nan, Wang, Xiaohong. 2022. Case Report: The novel hemizygous mutation in the SSR4 gene caused congenital disorder of glycosylation type iy: A case study and literature review. In Frontiers in genetics, 13, 955732. doi:10.3389/fgene.2022.955732. https://pubmed.ncbi.nlm.nih.gov/36386804/
5. Zhang, Jiaqi, Jia, Fang, Li, Chuqiao, Song, Shunzhe, Gong, Aixia. 2025. Unveiling SSR4: a promising biomarker in esophageal squamous cell carcinoma. In Frontiers in immunology, 16, 1544154. doi:10.3389/fimmu.2025.1544154. https://pubmed.ncbi.nlm.nih.gov/40066443/
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. Sun, Wenqiang, Jin, Xinyun, Zhu, Xueping. 2024. A novel SSR4 variant associated with congenital disorder of glycosylation: a case report and related analysis. In Frontiers in genetics, 15, 1402883. doi:10.3389/fgene.2024.1402883. https://pubmed.ncbi.nlm.nih.gov/39086474/