1. Karasu, Nilgun, Acer, Hamit, Akalin, Hilal, Canpolat, Mehmet, Dundar, Munis. 2024. Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy. In Journal of neurogenetics, 38, 102-111. doi:10.1080/01677063.2024.2407332. https://pubmed.ncbi.nlm.nih.gov/39321203/
2. Li, Zhenkun, Li, Yanmeng, Ouyang, Qin, Li, Xiaojin, Huang, Jian. 2022. Exosome-derived GTF2H2 from Huh7 cells can inhibit endothelial cell viability, migration, tube formation, and permeability. In Tissue & cell, 79, 101922. doi:10.1016/j.tice.2022.101922. https://pubmed.ncbi.nlm.nih.gov/36116407/
3. Hu, Ling, Yin, Wei, Ma, Yao, Zhang, Qiushi, Xu, Qingbang. 2023. Gene expression signature of human neuropathic pain identified through transcriptome analysis. In Frontiers in genetics, 14, 1127167. doi:10.3389/fgene.2023.1127167. https://pubmed.ncbi.nlm.nih.gov/36816032/
4. Liu, Zhidai, Zhang, Penghui, He, Xiaoyan, Hong, Siqi, Zou, Lin. 2016. New multiplex real-time PCR approach to detect gene mutations for spinal muscular atrophy. In BMC neurology, 16, 141. doi:10.1186/s12883-016-0651-y. https://pubmed.ncbi.nlm.nih.gov/27534852/
5. Theodorou, L, Nicolaou, P, Koutsou, P, Zamba-Papanicolaou, E, Christodoulou, K. 2015. Genetic findings of Cypriot spinal muscular atrophy patients. In Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 36, 1829-34. doi:10.1007/s10072-015-2263-5. https://pubmed.ncbi.nlm.nih.gov/26017350/
智鼠故事 
