1. Zhen, Ru, Moo, Chingyee, Zhao, Zhenzhen, Shi, Jiahai, Chen, Caiyong. . Wdr26 regulates nuclear condensation in developing erythroblasts. In Blood, 135, 208-219. doi:10.1182/blood.2019002165. https://pubmed.ncbi.nlm.nih.gov/31945154/
2. Onea, Gabriel, Ghahramani, Alireza, Wang, Xu, Bérubé, Nathalie G, Schild-Poulter, Caroline. 2025. WDR26 depletion alters chromatin accessibility and gene expression profiles in mammalian cells. In Genomics, 117, 111001. doi:10.1016/j.ygeno.2025.111001. https://pubmed.ncbi.nlm.nih.gov/39837355/
3. Hu, Jiacheng, Xu, Mingming, Zhu, Xiaobo, Zhang, Yu. 2022. Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability. In Genes, 13, . doi:10.3390/genes13050813. https://pubmed.ncbi.nlm.nih.gov/35627197/
4. Gunasekaran, Pradeep Kumar, Kumar, Ashna, Uk, Kandha Kumar, Tiwari, Sarbesh, Saini, Lokesh. 2023. Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene. In Indian journal of pediatrics, 91, 317. doi:10.1007/s12098-023-04970-6. https://pubmed.ncbi.nlm.nih.gov/38052954/
5. Pavinato, Lisa, Trajkova, Slavica, Grosso, Enrico, Keller, Roberto, Brusco, Alfredo. 2021. Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. In American journal of medical genetics. Part A, 185, 1712-1720. doi:10.1002/ajmg.a.62157. https://pubmed.ncbi.nlm.nih.gov/33675273/
6. Yang, Qi, Zhou, Xunzhao, Yi, Sheng, Qin, Zailong, Luo, Jingsi. 2024. Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients. In Frontiers in pediatrics, 12, 1429586. doi:10.3389/fped.2024.1429586. https://pubmed.ncbi.nlm.nih.gov/39363971/
7. Xia, Meiling, Yan, Rui, Wang, Wenjuan, Wan, Bo, Xu, Xingshun. 2023. GID complex regulates the differentiation of neural stem cells by destabilizing TET2. In Frontiers of medicine, 17, 1204-1218. doi:10.1007/s11684-023-1007-9. https://pubmed.ncbi.nlm.nih.gov/37707676/
8. Cospain, Auriane, Schaefer, Elise, Faoucher, Marie, Fradin, Mélanie, Lavillaureix, Alinoë. 2021. Skraban-Deardorff syndrome: Six new cases of WDR26-related disease and expansion of the clinical phenotype. In Clinical genetics, 99, 732-739. doi:10.1111/cge.13933. https://pubmed.ncbi.nlm.nih.gov/33506510/
智鼠故事 
