1. Li, Ren-Ke, Li, Huan, Tian, Mao-Qiang, Li, Bin, Shu, Xiao-Mei. 2023. Investigation of FRMPD4 variants associated with X-linked epilepsy. In Seizure, 116, 45-50. doi:10.1016/j.seizure.2023.05.014. https://pubmed.ncbi.nlm.nih.gov/37330374/
2. Trujillano, Daniel, Bertoli-Avella, Aida M, Kumar Kandaswamy, Krishna, Rolfs, Arndt, Abou Jamra, Rami. 2016. Clinical exome sequencing: results from 2819 samples reflecting 1000 families. In European journal of human genetics : EJHG, 25, 176-182. doi:10.1038/ejhg.2016.146. https://pubmed.ncbi.nlm.nih.gov/27848944/
3. Piard, Juliette, Hu, Jia-Hua, Campeau, Philippe M, Wang, Tao, Worley, Paul F. . FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis. In Human molecular genetics, 27, 589-600. doi:10.1093/hmg/ddx426. https://pubmed.ncbi.nlm.nih.gov/29267967/
4. Liu, Bin, Xiang, Yu, Guo, Weihua. 2024. Potential role of CTNNA3 and FRMPD4 in vascular tumorous thrombosis of colon adenocarcinoma. In Indian journal of pathology & microbiology, 67, 775-786. doi:10.4103/ijpm.ijpm_288_23. https://pubmed.ncbi.nlm.nih.gov/38727409/
5. Kim, Stuart K, Nguyen, Condor, Jones, Kevin B, Tashjian, Robert Z. 2021. A genome-wide association study for shoulder impingement and rotator cuff disease. In Journal of shoulder and elbow surgery, 30, 2134-2145. doi:10.1016/j.jse.2020.11.025. https://pubmed.ncbi.nlm.nih.gov/33482370/
智鼠故事 
