1. Wang, Zhao-Wei, Wang, Li-Ping, Du, Ye, Liu, Qi. 2021. Mutations in NOTCH3 Gene may Promote the Clinical Presentation of Spinocerebellar Ataxia Type 37 Caused by Mutations in DAB1 Gene. In Frontiers in molecular biosciences, 8, 668312. doi:10.3389/fmolb.2021.668312. https://pubmed.ncbi.nlm.nih.gov/34222332/
2. Rizikalo, Azer, Maglica, Mirko, Kelam, Nela, Mišković, Josip, Vukojević, Katarina. 2024. Unraveling the Impact of Dab1 Gene Silencing on the Expression of Autophagy Markers in Lung Development. In Life (Basel, Switzerland), 14, . doi:10.3390/life14030316. https://pubmed.ncbi.nlm.nih.gov/38541642/
3. Honda, Takao, Hirota, Yuki, Nakajima, Kazunori. 2023. Heterozygous Dab1 Null Mutation Disrupts Neocortical and Hippocampal Development. In eNeuro, 10, . doi:10.1523/ENEURO.0433-22.2023. https://pubmed.ncbi.nlm.nih.gov/36941061/
4. Lambert de Rouvroit, C, Goffinet, A M. . Neuronal migration. In Mechanisms of development, 105, 47-56. doi:. https://pubmed.ncbi.nlm.nih.gov/11429281/
5. Bar, Isabelle, Tissir, Fadel, Lambert de Rouvroit, Catherine, De Backer, Olivier, Goffinet, Andre M. 2002. The gene encoding disabled-1 (DAB1), the intracellular adaptor of the Reelin pathway, reveals unusual complexity in human and mouse. In The Journal of biological chemistry, 278, 5802-12. doi:. https://pubmed.ncbi.nlm.nih.gov/12446734/
6. Gao, Hui, Tao, Yu, He, Qin, Song, Fan, Saffen, David. 2015. Functional enrichment analysis of three Alzheimer's disease genome-wide association studies identities DAB1 as a novel candidate liability/protective gene. In Biochemical and biophysical research communications, 463, 490-5. doi:10.1016/j.bbrc.2015.05.044. https://pubmed.ncbi.nlm.nih.gov/26028559/
智鼠故事 
