1. Zocchi, Riccardo, Bellacchio, Emanuele, Piccione, Michela, Bertini, Enrico, Sferra, Antonella. 2023. Novel loss of function mutation in TUBA1A gene compromises tubulin stability and proteostasis causing spastic paraplegia and ataxia. In Frontiers in cellular neuroscience, 17, 1162363. doi:10.3389/fncel.2023.1162363. https://pubmed.ncbi.nlm.nih.gov/37435044/
2. Veldman, Matthew B, Bemben, Michael A, Goldman, Daniel. 2010. Tuba1a gene expression is regulated by KLF6/7 and is necessary for CNS development and regeneration in zebrafish. In Molecular and cellular neurosciences, 43, 370-83. doi:10.1016/j.mcn.2010.01.004. https://pubmed.ncbi.nlm.nih.gov/20123021/
3. Buscaglia, Georgia, Northington, Kyle R, Moore, Jeffrey K, Bates, Emily Anne. 2020. Reduced TUBA1A Tubulin Causes Defects in Trafficking and Impaired Adult Motor Behavior. In eNeuro, 7, . doi:10.1523/ENEURO.0045-20.2020. https://pubmed.ncbi.nlm.nih.gov/32184299/
4. Buscaglia, Georgia, Northington, Kyle R, Aiken, Jayne, Hoff, Katelyn J, Bates, Emily A. 2022. Bridging the Gap: The Importance of TUBA1A α-Tubulin in Forming Midline Commissures. In Frontiers in cell and developmental biology, 9, 789438. doi:10.3389/fcell.2021.789438. https://pubmed.ncbi.nlm.nih.gov/35127710/
5. Jin, Sheng Chih, Lewis, Sara A, Bakhtiari, Somayeh, MacLennan, Alastair H, Kruer, Michael C. 2020. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy. In Nature genetics, 52, 1046-1056. doi:10.1038/s41588-020-0695-1. https://pubmed.ncbi.nlm.nih.gov/32989326/