1. Ma, X Rosa, Prudencio, Mercedes, Koike, Yuka, Petrucelli, Leonard, Gitler, Aaron D. 2022. TDP-43 represses cryptic exon inclusion in the FTD-ALS gene UNC13A. In Nature, 603, 124-130. doi:10.1038/s41586-022-04424-7. https://pubmed.ncbi.nlm.nih.gov/35197626/
2. Willemse, Sean W, Harley, Peter, van Eijk, Ruben P A, Fratta, Pietro, van Es, Michael A. 2023. UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target. In Journal of neurology, neurosurgery, and psychiatry, 94, 649-656. doi:10.1136/jnnp-2022-330504. https://pubmed.ncbi.nlm.nih.gov/36737245/
3. Brown, Anna-Leigh, Wilkins, Oscar G, Keuss, Matthew J, Ward, Michael E, Fratta, Pietro. 2022. TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A. In Nature, 603, 131-137. doi:10.1038/s41586-022-04436-3. https://pubmed.ncbi.nlm.nih.gov/35197628/
4. Chen, Xi, Chu, Heling, Dong, Yi. 2022. UNC13A Gene Brings New Hope for ALS Disease-Modifying Drugs. In Neuroscience bulletin, 38, 1431-1434. doi:10.1007/s12264-022-00924-8. https://pubmed.ncbi.nlm.nih.gov/35907106/
5. Ohno, Kinji, Ohkawara, Bisei, Shen, Xin-Ming, Selcen, Duygu, Engel, Andrew G. 2023. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review. In International journal of molecular sciences, 24, . doi:10.3390/ijms24043730. https://pubmed.ncbi.nlm.nih.gov/36835142/
6. Keuss, Matthew J, Harley, Peter, Ryadnov, Eugeni, Burrone, Juan, Fratta, Pietro. 2024. Loss of TDP-43 induces synaptic dysfunction that is rescued by UNC13A splice-switching ASOs. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.06.20.599684. https://pubmed.ncbi.nlm.nih.gov/38979232/
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