1. Ayaz, Akif, Uzunhan, Tugce Aksu, Aydin, Kursad. 2022. Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia. In Brain & development, 44, 329-335. doi:10.1016/j.braindev.2022.01.002. https://pubmed.ncbi.nlm.nih.gov/35090779/
2. Zhu, Liwen, Bai, Wenke, Cheng, Qianyi, Fang, Jianpei. . ZNF384-Related Fusion Genes in Acute Lymphoblastic Leukemia. In Cancer control : journal of the Moffitt Cancer Center, 30, 10732748231182787. doi:10.1177/10732748231182787. https://pubmed.ncbi.nlm.nih.gov/37306722/
3. Kestle, John R W, Lee, Amy, Anderson, Richard C E, Imahiyerobo, Thomas, Siddiqi, Faizi A. 2018. Variation in the management of isolated craniosynostosis: a survey of the Synostosis Research Group. In Journal of neurosurgery. Pediatrics, 22, 627-631. doi:10.3171/2018.7.PEDS18132. https://pubmed.ncbi.nlm.nih.gov/30215587/
4. Baker, Cordell M, Ravindra, Vijay M, Gociman, Barbu, Imahiyerobo, Thomas, Kestle, John R W. . Management of sagittal synostosis in the Synostosis Research Group: baseline data and early outcomes. In Neurosurgical focus, 50, E3. doi:10.3171/2021.1.FOCUS201029. https://pubmed.ncbi.nlm.nih.gov/33794498/
5. Liu, Dingsheng, Zuo, Xiaojia, Zhang, Peng, Lu, Changlian, Gu, Xuefeng. 2021. The Novel Regulatory Role of lncRNA-miRNA-mRNA Axis in Amyotrophic Lateral Sclerosis: An Integrated Bioinformatics Analysis. In Computational and mathematical methods in medicine, 2021, 5526179. doi:10.1155/2021/5526179. https://pubmed.ncbi.nlm.nih.gov/33953791/
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