1. Birtele, Marcella, Del Dosso, Ashley, Xu, Tiantian, Coba, Marcelo P, Quadrato, Giorgia. 2023. Non-synaptic function of the autism spectrum disorder-associated gene SYNGAP1 in cortical neurogenesis. In Nature neuroscience, 26, 2090-2103. doi:10.1038/s41593-023-01477-3. https://pubmed.ncbi.nlm.nih.gov/37946050/
2. Turner, Tychele N, Wilfert, Amy B, Bakken, Trygve E, Retterer, Kyle, Eichler, Evan E. 2019. Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders. In American journal of human genetics, 105, 1274-1285. doi:10.1016/j.ajhg.2019.11.003. https://pubmed.ncbi.nlm.nih.gov/31785789/
3. Tian, X J, Fang, F, Ding, C H, Han, T L, Deng, J. . [Clinical characteristics and gene analysis of SYNGAP1-related epilepsy in children]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 59, 1059-1064. doi:10.3760/cma.j.cn112140-20210430-00369. https://pubmed.ncbi.nlm.nih.gov/34856666/
4. Agarwal, Mudit, Johnston, Michael V, Stafstrom, Carl E. 2019. SYNGAP1 mutations: Clinical, genetic, and pathophysiological features. In International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 78, 65-76. doi:10.1016/j.ijdevneu.2019.08.003. https://pubmed.ncbi.nlm.nih.gov/31454529/
5. Anderson, Joseph S, Lodigiani, Alyse L, Barbaduomo, Camilla M, Beegle, Julie R. . Hematopoietic stem cell gene therapy for the treatment of SYNGAP1-related non-specific intellectual disability. In The journal of gene medicine, 26, e3717. doi:10.1002/jgm.3717. https://pubmed.ncbi.nlm.nih.gov/38967915/
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