1. Li, Muquan, Luo, Shuanghong, Zhuo, Zhiqiang, Shu, Min. 2023. Two cases of pediatric primary immunodeficiency caused by a familial moesin(MSN)gene mutation. In Clinical immunology (Orlando, Fla.), 258, 109858. doi:10.1016/j.clim.2023.109858. https://pubmed.ncbi.nlm.nih.gov/38052292/
2. Sun, Bijun, Liu, Luyao, Han, Lingli, Wang, Xiaochuan, Sun, Jinqiao. 2024. Novel Mutation in the Moesin (MSN) Gene Leads to Immunodeficiency with Epstein-Barr Virus (EBV) Infection and Dermatomyositis-Like Symptoms. In Journal of clinical immunology, 44, 155. doi:10.1007/s10875-024-01755-0. https://pubmed.ncbi.nlm.nih.gov/38922539/
3. Shamseldin, Hanan E, AlAbdi, Lama, Maddirevula, Sateesh, Gao, Xin, Alkuraya, Fowzan S. 2021. Lethal variants in humans: lessons learned from a large molecular autopsy cohort. In Genome medicine, 13, 161. doi:10.1186/s13073-021-00973-0. https://pubmed.ncbi.nlm.nih.gov/34645488/
4. Yang, Yongchang, Xu, Xing, Xie, Yang, Wang, Xiaoguang, Jin, Xun. . Identification of Neural Progenitor Cell-associated Chemoradiotherapy Resistance Gene Set (ARL4C, MSN, TNFAIP6) for Prognosis of Glioma. In Current pharmaceutical design, 28, 2189-2202. doi:10.2174/1381612828666220617085508. https://pubmed.ncbi.nlm.nih.gov/35718975/
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