1. Duz, Mehmet Bugrahan, Topak, Ali. . Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature review. In Clinical dysmorphology, 29, 167-172. doi:10.1097/MCD.0000000000000329. https://pubmed.ncbi.nlm.nih.gov/32639237/
2. Baidoe-Ansah, David, Sakib, Sadman, Jia, Shaobo, Kaushik, Rahul, Dityatev, Alexander. 2022. Aging-Associated Changes in Cognition, Expression and Epigenetic Regulation of Chondroitin 6-Sulfotransferase Chst3. In Cells, 11, . doi:10.3390/cells11132033. https://pubmed.ncbi.nlm.nih.gov/35805117/
3. Mughal, Tufail Akbar, Asim, Muhammad, Gillani, Syed Haseeb Ul Hassan, Shujaat, Kulsoom, Gilani, Syed Zohaib Tayyab. 2024. A Novel Missense Variant in the CHST3 Underlies Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations. In Molecular syndromology, 15, 355-361. doi:10.1159/000538039. https://pubmed.ncbi.nlm.nih.gov/39359945/
4. Guan, Yunzhi, Sun, Chi, Zou, Fei, Jiang, Jianyuan, Ma, Xiaosheng. 2021. Carbohydrate sulfotransferase 3 (CHST3) overexpression promotes cartilage endplate-derived stem cells (CESCs) to regulate molecular mechanisms related to repair of intervertebral disc degeneration by rat nucleus pulposus. In Journal of cellular and molecular medicine, 25, 6006-6017. doi:10.1111/jcmm.16440. https://pubmed.ncbi.nlm.nih.gov/33993645/
5. Feng, Lili, Li, Ying, Li, Ying, Yuan, Dai, Fan, Juan. . Whole exome sequencing detects CHST3 mutation in patient with acute promyelocytic leukemia: A case report. In Medicine, 97, e12214. doi:10.1097/MD.0000000000012214. https://pubmed.ncbi.nlm.nih.gov/30200136/
6. Waryah, A M, Shahzad, M, Shaikh, H, Riazuddin, S, Ahmed, Z M. 2015. A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. In Clinical genetics, 90, 90-5. doi:10.1111/cge.12694. https://pubmed.ncbi.nlm.nih.gov/26572954/