1. Madaan, Priyanka, Kaushal, Yashovardhan, Srivastava, Priyanka, Ahuja, Chirag, Sankhyan, Naveen. 2022. Delineating the epilepsy phenotype of NRROS-related microgliopathy: A case report and literature review. In Seizure, 100, 15-20. doi:10.1016/j.seizure.2022.06.001. https://pubmed.ncbi.nlm.nih.gov/35716448/
2. Kim, Jung Ha, Kim, Kabsun, Kim, Inyoung, Seong, Semun, Kim, Nacksung. 2015. NRROS Negatively Regulates Osteoclast Differentiation by Inhibiting RANKL-Mediated NF-N:B and Reactive Oxygen Species Pathways. In Molecules and cells, 38, 904-10. doi:10.14348/molcells.2015.0177. https://pubmed.ncbi.nlm.nih.gov/26442864/
3. Dong, Xiaomin, Tan, Natalie B, Howell, Katherine B, Christodoulou, John, White, Susan M. 2020. Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification. In American journal of human genetics, 106, 559-569. doi:10.1016/j.ajhg.2020.02.014. https://pubmed.ncbi.nlm.nih.gov/32197075/
4. Tang, Xianfa, Fang, Fang, Yang, Jingjing, Wang, Liyun, Zhang, Anping. 2019. Association Study Reveals One Susceptibility Locus with Vitiligo in the Chinese Han Population. In Genetic testing and molecular biomarkers, 23, 791-796. doi:10.1089/gtmb.2019.0129. https://pubmed.ncbi.nlm.nih.gov/31644309/
5. Ishaq, Rafaqat, Ilyas, Muhammad, Habiba, Umme, Shaiq, Pakeeza Arzoo, Ahmed, Zubair M. 2023. Whole Exome Sequencing Reveals Clustering of Variants of Known Vitiligo Genes in Multiplex Consanguineous Pakistani Families. In Genes, 14, . doi:10.3390/genes14051118. https://pubmed.ncbi.nlm.nih.gov/37239478/
智鼠故事 
