1. Nudel, Ron. 2016. An investigation of NFXL1, a gene implicated in a study of specific language impairment. In Journal of neurodevelopmental disorders, 8, 13. doi:10.1186/s11689-016-9146-9. https://pubmed.ncbi.nlm.nih.gov/27053962/
2. Zhu, Qiao-Yun, Zhang, Lin-Lin, Liu, Jian-Xiang. . NFXL1 functions as a transcriptional activator required for thermotolerance at reproductive stage in Arabidopsis. In Journal of integrative plant biology, 66, 54-65. doi:10.1111/jipb.13604. https://pubmed.ncbi.nlm.nih.gov/38141041/
3. Villanueva, Pía, Nudel, Ron, Hoischen, Alexander, Fisher, Simon E, Newbury, Dianne F. 2015. Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. In PLoS genetics, 11, e1004925. doi:10.1371/journal.pgen.1004925. https://pubmed.ncbi.nlm.nih.gov/25781923/
4. Andres, Erin M, Neely, Heather L, Hafeez, Huma, Basra, M Asim Raza, Raza, Muhammad Hashim. 2021. Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment. In Meta gene, 30, . doi:10.1016/j.mgene.2021.100966. https://pubmed.ncbi.nlm.nih.gov/34540591/
智鼠故事 
