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2. Wu, Dengchang, Ji, Caihong, Chen, Zhongqin, Wang, Kang. 2020. Novel NEXMIF gene pathogenic variant in a female patient with refractory epilepsy and intellectual disability. In American journal of medical genetics. Part A, 182, 2765-2772. doi:10.1002/ajmg.a.61848. https://pubmed.ncbi.nlm.nih.gov/32924309/
3. Qi, Hongli, Pan, Dongju, Zhang, Ying, Zhang, Xie, Fu, Tingting. . NEXMIF Combined with KIDINS220 Gene Mutation Caused Neurodevelopmental Disorder and Epilepsy: One Case Report. In Actas espanolas de psiquiatria, 52, 588-594. doi:10.62641/aep.v52i4.1625. https://pubmed.ncbi.nlm.nih.gov/39129698/
4. Gilbert, James, O'Connor, Margaret, Templet, Sebastian, Xu, Weifeng, Man, Heng-Ye. 2019. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 40, 237-254. doi:10.1523/JNEUROSCI.0222-19.2019. https://pubmed.ncbi.nlm.nih.gov/31704787/
5. Stekelenburg, Caroline, Blouin, Jean-Louis, Santoni, Federico, Maechler, Pierre, Schwitzgebel, Valerie M. 2022. Loss of Nexmif results in the expression of phenotypic variability and loss of genomic integrity. In Scientific reports, 12, 13815. doi:10.1038/s41598-022-17845-1. https://pubmed.ncbi.nlm.nih.gov/35970867/
6. Alarcon-Martinez, Tuğba, Khan, Ayesha, Myers, Kenneth A. 2019. Torpedo Maculopathy Associated with NEXMIF Mutation. In Molecular syndromology, 10, 229-233. doi:10.1159/000498835. https://pubmed.ncbi.nlm.nih.gov/31602197/
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