1. Alazami, Anas M, Patel, Nisha, Shamseldin, Hanan E, Monies, Dorota M, Alkuraya, Fowzan S. 2014. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. In Cell reports, 10, 148-61. doi:10.1016/j.celrep.2014.12.015. https://pubmed.ncbi.nlm.nih.gov/25558065/
2. Lin, Haifan, Matzuk, Martin M. 2015. Poreless eggshells. In The Journal of clinical investigation, 125, 4005-7. doi:10.1172/JCI84692. https://pubmed.ncbi.nlm.nih.gov/26485282/
3. Park, Eujin, Ahn, Yo Han, Kang, Hee Gyung, Tsukaguchi, Hiroyasu, Cheong, Hae Il. . NUP107 mutations in children with steroid-resistant nephrotic syndrome. In Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 32, 1013-1017. doi:10.1093/ndt/gfw103. https://pubmed.ncbi.nlm.nih.gov/27190346/
4. Park, Eujin, Lee, Chung, Kim, Nayoung K D, Park, Woong-Yang, Cheong, Hae Il. 2020. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. In Journal of clinical medicine, 9, . doi:10.3390/jcm9062013. https://pubmed.ncbi.nlm.nih.gov/32604935/
5. Han, Yanxinli, Sha, Hongyu, Yang, Yuan, Zhang, Yu, Zhou, Jianhua. 2024. Mutations in the NUP93, NUP107 and NUP160 genes cause steroid-resistant nephrotic syndrome in Chinese children. In Italian journal of pediatrics, 50, 81. doi:10.1186/s13052-024-01656-3. https://pubmed.ncbi.nlm.nih.gov/38650033/
智鼠故事 
