1. Song, Danyu, Dai, Yi, Chen, Xiaoyu, Toda, Tatsushi, Xiong, Hui. 2021. Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients. In Clinical genetics, 99, 384-395. doi:10.1111/cge.13886. https://pubmed.ncbi.nlm.nih.gov/33200426/
2. Wang, Peng, Jin, Pengzhen, Zhu, Linyan, Xu, Yanfei, Dong, Minyue. 2022. Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene. In The journal of gene medicine, 24, e3417. doi:10.1002/jgm.3417. https://pubmed.ncbi.nlm.nih.gov/35338537/
3. Hedberg, Carola, Oldfors, Anders, Darin, Niklas. 2013. B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations. In European journal of human genetics : EJHG, 22, 707-10. doi:10.1038/ejhg.2013.223. https://pubmed.ncbi.nlm.nih.gov/24084573/
4. Zeng, Li'na, Lin, Li, Zhang, Yan, Xu, Qing, Lin, Congshan. . [Genetic analysis of a Chinese family affected with α-dystroglycanopathy due to variant of B3GALNT2 gene]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 40, 802-806. doi:10.3760/cma.j.cn511374-20220624-00426. https://pubmed.ncbi.nlm.nih.gov/37368380/
5. Matsuo, Taisuke, Komatsu, Masato, Yoshimaru, Tetsuro, Sasa, Mitsunori, Katagiri, Toyomasa. 2013. Involvement of B3GALNT2 overexpression in the cell growth of breast cancer. In International journal of oncology, 44, 427-34. doi:10.3892/ijo.2013.2187. https://pubmed.ncbi.nlm.nih.gov/24285400/
智鼠故事 
