1. Zhang, Zhujun, Yagi, Mariko, Okizuka, Yo, Takeshima, Yasuhiro, Matsuo, Masafumi. 2009. Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene. In Journal of human genetics, 54, 466-73. doi:10.1038/jhg.2009.63. https://pubmed.ncbi.nlm.nih.gov/19609279/
2. Montani, Caterina, Gritti, Laura, Beretta, Stefania, Verpelli, Chiara, Sala, Carlo. 2018. The Synaptic and Neuronal Functions of the X-Linked Intellectual Disability Protein Interleukin-1 Receptor Accessory Protein Like 1 (IL1RAPL1). In Developmental neurobiology, 79, 85-95. doi:10.1002/dneu.22657. https://pubmed.ncbi.nlm.nih.gov/30548231/
3. Piton, Amélie, Michaud, Jacques L, Peng, Huashan, Carbonetto, Salvatore, Rouleau, Guy A. 2008. Mutations in the calcium-related gene IL1RAPL1 are associated with autism. In Human molecular genetics, 17, 3965-74. doi:10.1093/hmg/ddn300. https://pubmed.ncbi.nlm.nih.gov/18801879/
4. Ramos-Brossier, Mariana, Montani, Caterina, Lebrun, Nicolas, Sala, Carlo, Billuart, Pierre. 2014. Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis. In Human molecular genetics, 24, 1106-18. doi:10.1093/hmg/ddu523. https://pubmed.ncbi.nlm.nih.gov/25305082/
5. Youngs, Erin L, Henkhaus, Rebecca, Hellings, Jessica A, Butler, Merlin G. 2011. IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. In European journal of medical genetics, 55, 32-6. doi:10.1016/j.ejmg.2011.08.004. https://pubmed.ncbi.nlm.nih.gov/21933724/
6. Montani, Caterina, Ramos-Brossier, Mariana, Ponzoni, Luisa, Billuart, Pierre, Sala, Carlo. 2017. The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 37, 6606-6627. doi:10.1523/JNEUROSCI.3775-16.2017. https://pubmed.ncbi.nlm.nih.gov/28576939/
7. Sun, Zhuo, Chadwick, Brian P. 2018. Loss of SETDB1 decompacts the inactive X chromosome in part through reactivation of an enhancer in the IL1RAPL1 gene. In Epigenetics & chromatin, 11, 45. doi:10.1186/s13072-018-0218-9. https://pubmed.ncbi.nlm.nih.gov/30103804/
8. Behnecke, Anne, Hinderhofer, Katrin, Bartsch, Oliver, Riess, Olaf, Moog, Ute. 2010. Intragenic deletions of IL1RAPL1: Report of two cases and review of the literature. In American journal of medical genetics. Part A, 155A, 372-9. doi:10.1002/ajmg.a.33656. https://pubmed.ncbi.nlm.nih.gov/21271657/
9. Dinopoulos, Argiris, Stefanou, Maria-Ioanna, Attilakos, Achilleas, Tsirouda, Maria, Papaevangelou, Vassiliki. 2014. A case of startle epilepsy associated with IL1RAPL1 gene deletion. In Pediatric neurology, 51, 271-4. doi:10.1016/j.pediatrneurol.2014.04.011. https://pubmed.ncbi.nlm.nih.gov/24950661/
10. Tabolacci, Elisabetta, Pomponi, M Grazia, Pietrobono, Roberta, Chiurazzi, Pietro, Neri, Giovanni. . A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family. In American journal of medical genetics. Part A, 140, 482-7. doi:. https://pubmed.ncbi.nlm.nih.gov/16470793/