1. Zrhidri, Abdelali, Jaouad, Imane Cherkaoui, Lyahyai, Jaber, El Mouatassim, Said, Sefiani, Abdelaziz. 2017. Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature. In Gene, 628, 190-193. doi:10.1016/j.gene.2017.07.011. https://pubmed.ncbi.nlm.nih.gov/28694206/
2. Zhu, Ying, Hu, Yunhong, Wang, Peipei, Sun, Leitao, Ruan, Shanming. 2023. Comprehensive bioinformatics and experimental analysis of SH3PXD2B reveals its carcinogenic effect in gastric carcinoma. In Life sciences, 326, 121792. doi:10.1016/j.lfs.2023.121792. https://pubmed.ncbi.nlm.nih.gov/37211344/
3. Yang, Bin, Tian, Cong, Zhang, Zhi-guang, Arnold, James E, Zheng, Qing Y. 2011. Sh3pxd2b mice are a model for craniofacial dysmorphology and otitis media. In PloS one, 6, e22622. doi:10.1371/journal.pone.0022622. https://pubmed.ncbi.nlm.nih.gov/21818352/
4. Kui, Xiang, Wang, Yan, Zhang, Cheng, Ke, Yang, Wang, Lin. 2021. Prognostic value of SH3PXD2B (Tks4) in human hepatocellular carcinoma: a combined multi-omics and experimental study. In BMC medical genomics, 14, 115. doi:10.1186/s12920-021-00963-6. https://pubmed.ncbi.nlm.nih.gov/33906640/
5. Wilson, Gabrielle R, Sunley, Jasmine, Smith, Katherine R, Bahlo, Melanie, Lockhart, Paul J. 2013. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. In European journal of human genetics : EJHG, 22, 741-7. doi:10.1038/ejhg.2013.229. https://pubmed.ncbi.nlm.nih.gov/24105366/